Decreased inward rectification of Kir2.1 channels is a novel mechanism underlying the short QT syndrome

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Bibliographic Details
Published inCardiovascular research Vol. 93; no. 4; pp. 535 - 536
Main Authors Casini, Simona, Postma, Alex V
Format Journal Article
LanguageEnglish
Published England 15.03.2012
Subjects
Animals
Female
Humans
Lown-Ganong-Levine Syndrome - genetics
Lown-Ganong-Levine Syndrome - physiopathology
Mutation - genetics
Potassium Channels, Inwardly Rectifying - genetics
Potassium Channels, Inwardly Rectifying - physiology
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Editorial-2
ObjectType-Commentary-1
ISSN:0008-6363
1755-3245
DOI:10.1093/cvr/cvs084