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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...
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| Publicado no: | Dis Model Mech |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Ltd
2019
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| Assuntos: | |
| Acesso em linha: | 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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