论文信息 - Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency - 字舞流文

Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency

G. Comi | F. Taroni | S. Baratta | C. Rodolico | A. Toscano | G. Vita | O. Musumeci | A. Bordoni | M. Aguennouz | M. Autunno