Intermediate forms of Charcot-Marie-Tooth neuropathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology,Molecular Medicine
Link
http://www.springerlink.com/index/pdf/10.1385/NMM:8:1-2:123
Reference52 articles.
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4. Birouk, N., Azzedine H., Dubourg, O., et al. (2003) Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. Arch. Neurol. 60, 598–604.
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