Associated Papers
Atrial fibrillation-a complex polygenetic disease.
Andersen JH et al.
European Journal of Human Genetics : Ejhg, 2021
33279945 (PubMed )
Supplement: 41431_2020_784_MOESM1_ESM.docx
Novel exon 1 protein-coding regions N-terminally extend human KCNE3 and KCNE4.
Abbott GW
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2016
KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulation.
Abbott GW
Gene, 2016
Arrhythmogenic KCNE gene variants: current knowledge and future challenges.
Crump SM et al.
Frontiers in Genetics, 2014
24478792 (PubMed )
Supplement: DataSheet1.DOCX
Mink S38G gene polymorphism and atrial fibrillation in the Chinese population: a meta-analysis of 1871 participants.
Li YY et al.
Thescientificworldjournal, 2014
Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus.
Sand PG et al.
Behavioral and Brain Functions : Bbf, 2011
Phenotypic manifestations of mutations in genes encoding subunits of cardiac potassium channels.
Shimizu W et al.
Circulation Research, 2011
[KCNE3 R53H substitution in familial atrial fibrillation].
Zhang DF et al.
Chinese Medical Journal, 2005
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