FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients

Autor: Awano, Hiroyuki, Saito, Yoshihiko, Shimizu, Mamiko, Sekiguchi, Kenji, Niijima, Shinichi, Matsuo, Masafumi, Maegaki, Yoshihiro, Izumi, Isho, Kikuchi, Chiya, Ishibashi, Masato, Okazaki, Tetsuya, Komaki, Hirofumi, Iijima, Kazumoto, Nishino, Ichizo
Zdroj: In Journal of Clinical Neuroscience October 2021 92:215-221
Databáze: ScienceDirect