Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families-Reference-Cited by-同舟云学术

Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families

Published:2001 Issue:1 Volume:18 Page:32-41
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Mostacciuolo M.L.,Righetti E.,Zortea M.,Bosello V.,Schiavon F.,Vallo L.,Merlini L.,Siciliano G.,Fabrizi G.M.,Rizzuto N.,Milani M.,Baratta S.,Taroni F.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference63 articles.

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

2. Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15

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

4. Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

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