N.P.3 05 Mitofusin 2 mutations are a major cause for autosomal dominant axonal CMT neuropathy

✍ Scribed by K. Verhoeven; K.G. Claeys; S. Züchner; J.M. Schröder; J.M. Vance; V. Timmerman; P. De Jonghe

• Book ID: 116792538
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 55 KB
• Volume: 16
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2006.05.081