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The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study
BACKGROUND: The gene family KCNE1-5, which encode modulating β-subunits of several repolarising K(+)-ion channels, has been associated with genetic cardiac diseases such as long QT syndrome, atrial fibrillation and Brugada syndrome. The minK peptide, encoded by KCNE1, is attached to the Z-disc of th...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3204304/ https://ncbi.nlm.nih.gov/pubmed/21967835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1477-5751-10-12 |
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