A Novel Mutation of GDAP1 Associated with Charcot-Marie-Tooth Disease in An Iranian Family

As a result of higher distributed consanguinity in the Mediterranean region and the Middle East, autosomal-recessive forms of Charcot-Marie-Tooth (ARCMT) are more common in these areas. CMT disease caused by mutations in the ganglioside-induced differentiation-associated protein 1 (GDAP1) gene is a...

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Bibliographic Details
Main Authors: MOHAMMADI PARGOO, Esmaeel, ARYANI, Omid, TONEKABONI, Seyyed Hassan, KAMALIDEHGHAN, Behnam, HOUSHMAND, Massoud
Format: Online
Published: Iranian Journal of Child Neurology 2012
Online Access:http://journals.sbmu.ac.ir/ijcn/article/view/3311

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