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

DOI
https://doi.org/10.1097/CM9.0000000000001425
Journal volume & issue
Vol. 134, no. 22
pp. 2753 – 2755

Abstract

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