Cellular Dysfunction of LQT5-MinK Mutants: Abnormalities of IKs, IKr and Trafficking in Long QT Syndrome-Reference-Cited by-同舟云学术

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Cellular Dysfunction of LQT5-MinK Mutants: Abnormalities of IKs, IKr and Trafficking in Long QT Syndrome

Published:1999-08-01 Issue:8 Volume:8 Page:1499-1507
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Bianchi L.,Shen Z.,Dennis A. T.,Priori S. G.,Napolitano C.,Ronchetti E.,Bryskin R.,Schwartz P. J.,Brown A. M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/8/8/1499/1655308/8-8-1499.pdf

Reference29 articles.

1. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death

2. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

3. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

4. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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