Complete Deletion of All α-Dystrobrevin Isoforms Does Not Reveal New Neuromuscular Junction Phenotype

The dystrophin glycoprotein complex (DGC) is critical for muscle stability, and mutations in DGC proteins lead to muscular dystrophy. The DGC also contributes to the maturation and maintenance of the neuromuscular junction (NMJ). The gene encoding the DGC protein α-dystrobrevin undergoes alternative...

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Detaylı Bibliyografya
Yayımlandı:Gene Expr
Asıl Yazarlar: Wang, Dongqing, Kelly, Bridget B., Albrecht, Douglas E., Adams, Marvin E., Froehner, Stanley C., Feng, Guoping
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cognizant Communication Corporation 2018
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042018/
https://ncbi.nlm.nih.gov/pubmed/17933218
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