A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2.
Qiu LL, Lin XD, Xu GR, Wang LL, Ye ZX, Lin F, Chen HZ, Lin MT, Cai NQ, Jin M, Xu LQ, Hu W, Wang N, Wang ZQ.
Qiu LL, et al. Among authors: wang ll, wang n, wang zq.
Chin Med J (Engl). 2021 Mar 23;134(22):2753-2755. doi: 10.1097/CM9.0000000000001425.
Chin Med J (Engl). 2021.
PMID: 34845997
Free PMC article.
No abstract available.