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Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot–Marie–Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE
Katell Beauvais, Alain Furby, Philippe LatourVolume:
16
Year:
2006
Language:
english
DOI:
10.1016/j.nmd.2005.09.008
File:
PDF, 139 KB
english, 2006