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Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Background: Myofibrillar myopathy is a group of hereditary neuromuscular disorders characterized by dissolution of myofibrils and abnormal intracellular accumulation of Z disc-related proteins. We aimed to characterize the clinical, physiological, pathohistological, and genetic features of Chinese m...

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Foilsithe in:Front Neurol
Main Authors: Luo, Yue-Bei, Peng, Yuyao, Lu, Yuling, Li, Qiuxiang, Duan, Huiqian, Bi, Fangfang, Yang, Huan
Formáid: Artigo
Teanga:Inglês
Foilsithe: Frontiers Media S.A. 2020
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7522348/
https://ncbi.nlm.nih.gov/pubmed/33041974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.01014
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