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

✍ Scribed by Katell Beauvais; Alain Furby; Philippe Latour

• Book ID: 116792381
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 139 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2005.09.008