Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease

Introduction: Charcot-Marie-Tooth disease (CMT) is the most frequent form of inherited neuropathy. In accordance with the inheritance pattern and degree of slowing of motor conduction velocity (MCV) of the median nerve, CMT encompasses five main forms: CMT1 (autosomal dominant [AD] or X-linked trans...

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Bibliographic Details
Main Authors: J. Berciano, T. Sevilla, C. Casasnovas, R. Sivera, J.J. Vílchez, J. Infante, C. Ramón, A.L. Pelayo-Negro, I. Illa
Format: Article
Language:English
Published: Elsevier España 2012-04-01
Series:Neurología (English Edition)
Online Access:http://www.sciencedirect.com/science/article/pii/S2173580812000417