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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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Détails bibliographiques
Publié dans:Gene Expr
Auteurs principaux: Wang, Dongqing, Kelly, Bridget B., Albrecht, Douglas E., Adams, Marvin E., Froehner, Stanley C., Feng, Guoping
Format: Artigo
Langue:Inglês
Publié: Cognizant Communication Corporation 2018
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042018/
https://ncbi.nlm.nih.gov/pubmed/17933218
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