TRPM4 non-selective cation channel variants in long QT syndrome

BACKGROUND: Long QT syndrome (LQTS) is an inherited arrhythmic disorder characterized by prolongation of the QT interval, a risk of syncope, and sudden death. There are already a number of causal genes in LQTS, but not all LQTS patients have an identified mutation, which suggests LQTS unknown genes....

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Detaylı Bibliyografya
Yayımlandı:BMC Med Genet
Asıl Yazarlar: Hof, Thomas, Liu, Hui, Sallé, Laurent, Schott, Jean-Jacques, Ducreux, Corinne, Millat, Gilles, Chevalier, Philippe, Probst, Vincent, Guinamard, Romain, Bouvagnet, Patrice
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2017
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5357330/
https://ncbi.nlm.nih.gov/pubmed/28315637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-017-0397-4
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