Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome-Reference-Cited by-同舟云学术

Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome

Published:2010-06 Issue:6 Volume:86 Page:872-880
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Yang Yanzong,Yang Yiqing,Liang Bo,Liu Jinqiu,Li Jun,Grunnet Morten,Olesen Søren-Peter,Rasmussen Hanne B.,Ellinor Patrick T.,Gao Lianjun,Lin Xiaoping,Li Li,Wang Lei,Xiao Junjie,Liu Yi,Liu Ying,Zhang Shulong,Liang Dandan,Peng Luying,Jespersen Thomas,Chen Yi-Han

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome;Wang;Cell,1995

5. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death;Mohler;Nature,2003

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