Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review

Zhang, G; Xu, M; Huang, TT; Lin, WX; Chen, JL; Chen, WY; Chang, XZ

Chang, XZ (corresponding author), Peking Univ First Hosp, Dept Pediat, No1 Xian Men St, Beijing 100034, Peoples R China.

BMC PEDIATRICS, 2021; 21 (1):

Abstract

BackgroundCentronuclear myopathy (CNM), a subtype of congenital myopathy (CM), is a group of clinical and genetically heterogeneous muscle disorders. ......

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