نتایج جستجو برای: kcne2 gene
تعداد نتایج: 1141429 فیلتر نتایج به سال:
Corrigendum to ‘‘Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia’’ [Experimental Hematology, Vol. 42, Issue 12, p1053–1058.e1] Grace Salsbury, Emma L. Cambridge, Zoe McIntyre, Mark J. Arends, Natasha A. Karp, Christopher Isherwood, Carl Shannon, Yvette Hooks, The Sanger Mouse Genetics Project, Ramiro Ramirez-Solis, David J. Adams, Jacqueline K. White, a...
Congenital long QT syndrome (cLQTS) is a genetic disorder predisposing to ventricular arrhythmia, syncope and sudden death. Over 700 different cLQTS-causing mutations in 13 genes are known. The genetic spectrum of LQTS in 44 South African cLQTS patients (23 known to carry the South African founder mutation p.A341V in KCNQ1) was established by screening for mutations in the coding regions of KCN...
INTRODUCTION rs9982601 (C>T) is a polymorphism of the noncoding region between the SLC5A3/MRPS6 and KCNE2 genes. It has been shown to be associated with early-onset myocardial infarction (MI) with T as a risk allele. OBJECTIVES The aim of our study was to investigate the association of the rs9982601 polymorphism with long-term overall mortality from MI and prevalence of MI in a Polish popul...
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