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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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Detalhes bibliográficos
Publicado no:Gene Expr
Main Authors: Wang, Dongqing, Kelly, Bridget B., Albrecht, Douglas E., Adams, Marvin E., Froehner, Stanley C., Feng, Guoping
Formato: Artigo
Idioma:Inglês
Publicado em: Cognizant Communication Corporation 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6042018/
https://ncbi.nlm.nih.gov/pubmed/17933218
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