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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Detaylı Bibliyografya
Asıl Yazarlar: Hedley, Paula L, Haundrup, Ole, Andersen, Paal S, Aidt, Frederik H, Jensen, Morten, Moolman-Smook, Johanna C, Bundgaard, Henning, Christiansen, Michael
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2011
Konular:
Research
Online Erişim: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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