Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. (Q31882183)

4 July 2017

Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. (English)

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4 July 2017

Barhoumi C

1

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4 July 2017

Amouri R

2

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4 July 2017

Ben Hamida C

3

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4 July 2017

Ben Hamida M

4

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4 July 2017

Machghoul S

5

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4 July 2017

Gueddiche M

6

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4 July 2017

Hentati F

7

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4 July 2017

1 January 2001

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4 July 2017

Neuromuscular Disorders

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4 July 2017

11

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4 July 2017

1

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4 July 2017

27-34

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Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

4 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Peroneal muscular atrophy with pyramidal features

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: studies of the HLA class II loci

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Structure and localization of the gene encoding human peripheral myelin protein 2 (PMP2).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Autosomal recessive forms of hereditary motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900162-0

7 January 2021

10.1016/S0960-8966(00)00162-0

Identifiers

DOI

1 reference

4 July 2017

1 reference