论文信息 - Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. - 字舞流文

Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.

M. Ridanpää | K. Pelin | H. Christen | H. Goebel | C. Wallgren‐Pettersson | M. de Visser | M. Ollikainen | K. Donner