Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

BACKGROUND: Dysferlinopathies are a group of autosomal recessive limb‐girdle muscular dystrophies (LGMDs) caused by mutations in DYSF (#603,009). This gene encodes a transmembrane protein called dysferlin. Since there are few reports on Iranian dysferlinopathy patients, we tried to identify the DYSF...

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Detalles Bibliográficos
Autores principales: Mojbafan, Marzieh, Tina, Shirzadeh, Zafarghandi Motlagh, Fatemeh, Surguchov, Andrei, Nilipour, Yalda, Zeinali, Sirous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900382/
https://www.ncbi.nlm.nih.gov/pubmed/31693312
http://dx.doi.org/10.1002/mgg3.1029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900382/
https://www.ncbi.nlm.nih.gov/pubmed/31693312
http://dx.doi.org/10.1002/mgg3.1029

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