Huntington's disease: a clinical, genetic and molecular model for polyglutamine repeat disorders (Q24676646)

scientific article

Language	Label	Description	Also known as
English	Huntington's disease: a clinical, genetic and molecular model for polyglutamine repeat disorders	scientific article

Statements

instance of

scholarly article

0 references

title

Huntington's disease: a clinical, genetic and molecular model for polyglutamine repeat disorders (English)

0 references

0 references

P S Harper

1

0 references

language of work or name

English

0 references

publication date

29 June 1999

0 references

published in

Philosophical Transactions of the Royal Society B

0 references

volume

354

0 references

issue

1386

0 references

page(s)

957-61

0 references

cites work

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

7 April 2017

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

28 September 2017

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1692597

retrieved

30 May 2018

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1098%2FRSTB.1999.0446

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The problem of anticipation in pedigrees of dystrophia myotonica

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1098%2FRSTB.1999.0446

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1098%2FRSTB.1999.0446

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1098/RSTB.1999.0446

0 references

0 references

0 references

ResearchGate publication ID

12866067

0 references

Huntington's disease: a clinical, genetic and molecular model for polyglutamine repeat disorders (Q24676646)

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Navigation menu

Huntington's disease: a clinical, genetic and molecular model for polyglutamine repeat disorders (Q24676646)

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Navigation menu

Search