α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

BACKGROUND: Sudden infant death syndrome (SIDS) is a leading cause of death during the first 6 months after birth. About 5%-10% of SIDS may stem from cardiac channelopathies like long QT syndrome (LQTS). We recently implicated mutations in α1-syntrophin (SNTA1) as a novel cause of LQTS, whereby muta...

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Main Authors: Cheng, Jianding, Van Norstrand, David W., Medeiros-Domingo, Argelia, Valdivia, Carmen, Tan, Bi-hua, Ye, Bin, Kroboth, Stacie, Vatta, Matteo, Tester, David J., January, Craig T., Makielski, Jonathan C., Ackerman, Michael J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2810855/
https://ncbi.nlm.nih.gov/pubmed/20009079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.109.891440
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