Cite
HARVARD Citation
Qiu, L. et al. (2021). A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2. Chinese medical journal. 134 (22), pp. 2753-2755. [Online].
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Qiu, L. et al. (2021). A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2. Chinese medical journal. 134 (22), pp. 2753-2755. [Online].