Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15

✍ Scribed by Nyamkhishig Sambuughin; Kumaraswamy Sivakumar; Badamjav Selenge; Hee Suk Lee; Daniel Friedlich; Damchaa Baasanjav; Marinos C Dalakas; Lev G Goldfarb

• Book ID: 119470133
• Publisher: Elsevier Science
• Year: 1998
• Tongue: English
• Weight: 165 KB
• Volume: 161
• Category: Article
• ISSN: 0022-510X
• DOI: 10.1016/s0022-510x(98)00264-0