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Alterations of Excitation–Contraction Coupling and Excitation Coupled Ca(2+) Entry in Human Myotubes Carrying CAV3 Mutations Linked to Rippling Muscle Disease
Rippling muscle disease is caused by mutations in the gene encoding caveolin-3 (CAV3), the muscle-specific isoform of the scaffolding protein caveolin, a protein involved in the formation of caveolae. In healthy muscle, caveolin-3 is responsible for the formation of caveolae, which are highly organi...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Subscription Services, Inc., A Wiley Company
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3132216/ https://ncbi.nlm.nih.gov/pubmed/21294223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21431 |
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