Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene

Limb girdle muscular dystrophy type 2I (LGMD2I) is an autosomal recessive muscular dystrophy that is rare in Asia and is caused by mutations in the fukutin-related protein gene (FKRP). The aim of this study was to determine if there are any characteristic features of muscle on magnetic resonance ima...

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Detalles Bibliográficos
Autores principales: Xie, Zhiying, Xiao, Jiangxi, Zheng, Yiming, Wang, Zhaoxia, Yuan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996470/
https://www.ncbi.nlm.nih.gov/pubmed/30003095
http://dx.doi.org/10.1155/2018/3710814

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996470/
https://www.ncbi.nlm.nih.gov/pubmed/30003095
http://dx.doi.org/10.1155/2018/3710814

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