A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
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通讯作者：
Zhiqiang Wang
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作者：
Liangliang Qiu;Xiaodan Lin;Guorong Xu;Lili Wang;Zhixian Ye;Feng Lin;Haizhu Chen;Minting Lin;Naiqing Cai;Ming Jin;Liuqing Xu;Wei Hu;Ning Wang;Zhiqiang Wang
