KCNE3 Mutation V17M Identified in a Patient with Lone Atrial Fibrillation | Zendy

Alicia Lundby | Zendy; Lasse Steen Ravn | Zendy; Jesper Hastrup Svendsen | Zendy; Stig Haunsø | Zendy; SørenPeter Olesen | Zendy; Nicole Schmitt | Zendy

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KCNE3 Mutation V17M Identified in a Patient with Lone Atrial Fibrillation

Author(s) -

Alicia Lundby,

Lasse Steen Ravn,

Jesper Hastrup Svendsen,

Stig Haunsø,

SørenPeter Olesen,

Nicole Schmitt

Publication year - 2008

Publication title -

cellular physiology and biochemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.486

H-Index - 87

eISSN - 1421-9778

pISSN - 1015-8987

DOI - 10.1159/000113746

Subject(s) - proband , missense mutation , mutation , medicine , ventricle , repolarization , genetics , short qt syndrome , biology , atrial fibrillation , cardiology , electrophysiology , endocrinology , long qt syndrome , gene , qt interval

Atrial fibrillation (AF) is the most common cardiac rhythm disorder with a lifetime risk for development of 25% for people aged 40 or older. In this study we aim for the functional assessment of a mutation in KCNE3 identified in a proband with early-onset lone AF.

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