SCN4B-Encoded Sodium Channel β4 Subunit in Congenital Long-QT Syndrome

BACKGROUND: Congenital long-QT syndrome (LQTS) is potentially lethal secondary to malignant ventricular arrhythmias and is caused predominantly by mutations in genes that encode cardiac ion channels. Nearly 25% of patients remain without a genetic diagnosis, and genes that encode cardiac channel reg...

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Hlavní autoři: Medeiros-Domingo, Argelia, Kaku, Toshihiko, Tester, David J., Iturralde-Torres, Pedro, Itty, Ajit, Ye, Bin, Valdivia, Carmen, Ueda, Kazuo, Canizales-Quinteros, Samuel, Tusié-Luna, Maria Teresa, Makielski, Jonathan C., Ackerman, Michael J.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2007
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3332546/
https://ncbi.nlm.nih.gov/pubmed/17592081
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCULATIONAHA.106.659086
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