Associated Papers
The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study.
Dai Q et al.
The Journal of International Advanced Otology, 2019
KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulation.
Abbott GW
Gene, 2016
The genetics of Ménière's disease.
Chiarella G et al.
The Application of Clinical Genetics, 2015
Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss.
Nishio N et al.
Life Sciences, 2013
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Ohno S et al.
Human Mutation, 2009
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
Tlili A et al.
Annals of Human Genetics, 2007
Potassium channel gene mutations rarely cause atrial fibrillation.
Ellinor PT et al.
Bmc Medical Genetics, 2006
Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3.
Doi K et al.
Orl; Journal for Oto-rhino-laryngology and Its Related Specialties, 2005
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