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Profiling of the muscle-specific dystroglycan interactome reveals the role of Hippo signaling in muscular dystrophy and age-dependent muscle atrophy

BACKGROUND: Dystroglycanopathies are a group of inherited disorders characterized by vast clinical and genetic heterogeneity and caused by abnormal functioning of the ECM receptor dystroglycan (Dg). Remarkably, among many cases of diagnosed dystroglycanopathies, only a small fraction can be linked d...

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Detalles Bibliográficos
Autores principales:	Yatsenko, Andriy S., Kucherenko, Mariya M., Xie, Yuanbin, Aweida, Dina, Urlaub, Henning, Scheibe, Renate J., Cohen, Shenhav, Shcherbata, Halyna R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971923/ https://www.ncbi.nlm.nih.gov/pubmed/31959160 http://dx.doi.org/10.1186/s12916-019-1478-3

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