Phenotypic variability of CMT4C in a French-Canadian kindred
Author:
Affiliation:
1. Department of Medicine; Neuromuscular Disease Clinic; McMaster University; Hamilton, HSC Room 2H22, 1200 Main Street West Ontario Canada L8N 3Z5
2. Division of Neurology; University of Ottawa; Ottawa Ontario Canada
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24640/fullpdf
Reference18 articles.
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2. Study on the gene and phenotypic characterization of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33;Gabreëls-Festen;J Neurol Neurosurg Psychiatry,1999
3. Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C;Yger;J Peripher Nerv Syst,2012
4. http://www.Molgen.ua.ac.be/CMTMutations/ 2012
5. Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster;Gosselin;Neuromuscul Disord,2008
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