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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Publicado en:Gene Expr
Autores principales: Wang, Dongqing, Kelly, Bridget B., Albrecht, Douglas E., Adams, Marvin E., Froehner, Stanley C., Feng, Guoping
Formato: Artigo
Lenguaje:Inglês
Publicado: Cognizant Communication Corporation 2018
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042018/
https://ncbi.nlm.nih.gov/pubmed/17933218
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