论文信息 - Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis - 字舞流文

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis

A. Pestronk | A. Goate | C. Cruchaga | C. Zaidman | J. Ravits | R. Baloh | M. Harms | P. Allred | Michael W. Baughn | R. Libby | Taha Bali | P. Cooper | J. Cady