Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region. (Q33910131)

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English	Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.	scientific article

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31 December 2019

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region (English)

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31 December 2019

Tourette syndrome

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based on heuristic

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Peristera Paschou

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31 December 2019

Mellissa Demille

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31 December 2019

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31 December 2019

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31 December 2019

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Y Feng

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31 December 2019

A J Pakstis

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31 December 2019

W C Speed

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31 December 2019

J R Kidd

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B Jaghori

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R Kurlan

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D L Pauls

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K K Kidd

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9 August 2004

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31 December 2019

American Journal of Human Genetics

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31 December 2019

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31 December 2019

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31 December 2019

545-560

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PMC publication ID

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31 December 2019

Understanding human DNA sequence variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Neurobiology of Tourette's syndrome: concepts of neuroanatomic localization and neurochemical abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

An update on the genetics of Gilles de la Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Diagnosing Tourette syndrome: is it a common disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

ProSAP/Shank postsynaptic density proteins interact with insulin receptor tyrosine kinase substrate IRSp53

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

A missense mutation in Tbce causes progressive motor neuronopathy in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Cdc42 induces filopodia by promoting the formation of an IRSp53:Mena complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Basal ganglia dysfunction in Tourette's syndrome: a new hypothesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Linkage disequilibrium in humans: models and data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Prospective, longitudinal study of tic, obsessive-compulsive, and attention-deficit/hyperactivity disorders in an epidemiological sample

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Tourette's syndrome: when habit-forming systems form habits of their own?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Current issues in Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Significant linkage for Tourette syndrome in a large French Canadian family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Function of tubulin binding proteins in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: associations with ADHD and family functioning. Attention Deficit Hyperactivity Disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Tubulin folding cofactor D is a microtubule destabilizing protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Tourette syndrome, associated conditions and the complexities of treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Genome scan for linkage to Gilles de la Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviors: Tourette syndrome, ADHD, pathological gambling, and substance abuse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Disentangling the overlap between Tourette's disorder and ADHD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Course of tic severity in Tourette syndrome: the first two decades

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Bipolar disorder in adult patients with Tourette's syndrome: a clinical study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Huntington's disease and dentatorubral-pallidoluysian atrophy: proteins, pathogenesis and pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Mouse and human neuronal pentraxin 1 (NPTX1): conservation, genomic structure, and chromosomal localization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Intermediate inheritance of Tourette syndrome, assuming assortative mating

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

The Yale Global Tic Severity Scale: initial testing of a clinician-rated scale of tic severity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Tourette's syndrome: current concepts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Hypothesis: homozygosity in Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

A family study of Gilles de la Tourette syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

5 July 2018

Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Narp and NP1 form heterocomplexes that function in developmental and activity-dependent synaptic plasticity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

The behavioral spectrum of tic disorders: a community-based study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Quality of Life (QOL) of patients with Gilles de la Tourette's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Comorbid Tourette's disorder and bipolar disorder: an etiologic perspective.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182043

29 October 2018

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for Genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced reciprocal translocation 46 XY, t(3:8)(p21.3 q24.1) in a case of Tourette syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased prevalence of the seven-repeat variant of the dopamine D4 receptor gene in patients with obsessive-compulsive disorder with tics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Candidate region for Gilles de la Tourette syndrome at 7q31

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tourette's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A twin study of Tourette syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Tourette's syndrome: report of a large pedigree and potential for linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation and linkage analyses of Tourette's syndrome and related disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom cohort study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilineal transmission in Tourette's syndrome families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/15303240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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31 December 2019

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31 December 2019

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