First familial limb-girdle muscular dystrophy 2L in China: Clinical, imaging, pathological, and genetic features

Limb-girdle muscular dystrophy 2L (LGMD2L) is mainly characterized by late adult onset, atrophy of proximal muscles, chronic progressive and asymmetric weakness, accompanied by increased creatine kinase (CK) levels, dystrophic pathological changes and electromyography showing myogenic damage. To dat...

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Detalles Bibliográficos
Autores principales: Hu, Bolin, Xiong, Li, Zhou, Yibiao, Lu, Xiaoqing, Xiong, Qianqian, Liu, Qing, Qi, Xueliang, Ding, Weijiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160217/
https://www.ncbi.nlm.nih.gov/pubmed/30235762
http://dx.doi.org/10.1097/MD.0000000000012506

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160217/
https://www.ncbi.nlm.nih.gov/pubmed/30235762
http://dx.doi.org/10.1097/MD.0000000000012506

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