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Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

Mutations affecting ryanodine receptor (RyR) calcium release channels commonly underlie congenital myopathies. Although these channels are known principally for their essential roles in muscle contractility, mutations in the human RYR1 gene result in a broad spectrum of phenotypes, including muscle...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Dis Model Mech
Egile Nagusiak: Chagovetz, Alexis A., Klatt Shaw, Dana, Ritchie, Erin, Hoshijima, Kazuyuki, Grunwald, David J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The Company of Biologists Ltd 2019
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6906632/
https://ncbi.nlm.nih.gov/pubmed/31383689
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.038844
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