Mutation in δ-Sg Gene in Familial Dilated Cardiomyopathy

BACKGROUND: Mutations in different genes including dystrophin-associated glycoprotein complex caused familial dilated cardiomyopathy which is a genetically heterogeneous disease. The δ-SG gene contains nine exons spanning a 433-kb region of genomic DNA. It encodes a 35-kDa, singlepass, and type II t...

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Detalles Bibliográficos
Autores principales: Asadi, Marzieh, Foo, Roger, Salehi, Ahmad Reza, Salehi, Rasoul, Samienasab, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360008/
https://www.ncbi.nlm.nih.gov/pubmed/28401079
http://dx.doi.org/10.4103/2277-9175.188492

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360008/
https://www.ncbi.nlm.nih.gov/pubmed/28401079
http://dx.doi.org/10.4103/2277-9175.188492

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