FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
- Resource Type
- Article
- Authors
- 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
- Source
- In Journal of Clinical Neuroscience October 2021 92:215-221
- Subject
- Language
- ISSN
- 0967-5868