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Chinese Medical Journal
(Nov 2021)
A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
Liang-Liang Qiu,
Xiao-Dan Lin,
Guo-Rong Xu,
Li-Li Wang,
Zhi-Xian Ye,
Feng Lin,
Hai-Zhu Chen,
Min-Ting Lin,
Nai-Qing Cai,
Ming Jin,
Liu-Qing Xu,
Wei Hu,
Ning Wang,
Zhi-Qiang Wang,
Li-Shao Guo
Affiliations
Liang-Liang Qiu
Xiao-Dan Lin
Guo-Rong Xu
Li-Li Wang
Zhi-Xian Ye
Feng Lin
Hai-Zhu Chen
Min-Ting Lin
Nai-Qing Cai
Ming Jin
Liu-Qing Xu
Wei Hu
Ning Wang
Zhi-Qiang Wang
Li-Shao Guo
DOI
https://doi.org/10.1097/CM9.0000000000001425
Journal volume & issue
Vol. 134, no. 22
pp. 2753 – 2755
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