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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Detalles Bibliográficos
Autores principales: Luo, Yue-Bei, Peng, Yuyao, Lu, Yuling, Li, Qiuxiang, Duan, Huiqian, Bi, Fangfang, Yang, Huan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522348/
https://www.ncbi.nlm.nih.gov/pubmed/33041974
http://dx.doi.org/10.3389/fneur.2020.01014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522348/
https://www.ncbi.nlm.nih.gov/pubmed/33041974
http://dx.doi.org/10.3389/fneur.2020.01014

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