Serum Cytokine Profile in a Patient Diagnosed with Dysferlinopathy

Limb-girdle muscular dystrophy type 2 (LGMD2B) is a mild form of dysferlinopathy, characterized by limb weakness and wasting. It is an autosomal recessive disease, with currently 140 mutations in the LGMD2B gene identified. Lack of functional dysferlin inhibits muscle fiber regeneration in voluntary...

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Detalles Bibliográficos
Autores principales: Khaiboullina, Svetlana F., Martynova, Ekaterina V., Bardakov, Sergey N., Mavlikeev, Mikhail O., Yakovlev, Ivan A., Isaev, Arthur A., Deev, Roman V., Rizvanov, Albert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406743/
https://www.ncbi.nlm.nih.gov/pubmed/28487742
http://dx.doi.org/10.1155/2017/3615354

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406743/
https://www.ncbi.nlm.nih.gov/pubmed/28487742
http://dx.doi.org/10.1155/2017/3615354

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