Open AccessA novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
Author(s) -
Liangliang Qiu,
Xiaodan Lin,
Guiyin Xu,
Lili Wang,
Zhixian Ye,
Feng Lin,
Hai-Zhu Chen,
Min Lin,
Nai-Qing Cai,
Ming Jin,
Litao Xu,
Wei Hu,
Ning Wang,
Zhiqiang Wang
Publication year - 2021
Publication title -
chinese medical journal/chinese medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 63
eISSN - 2542-5641
pISSN - 0366-6999
DOI - 10.1097/cm9.0000000000001425
Subject(s) - facioscapulohumeral muscular dystrophy , muscular dystrophy , genetics , biology , medicine