Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation-Reference-Cited by-同舟云学术

Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Published:2008-04 Issue:4 Volume:5 Page:553-561
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Bhuiyan Zahurul A.,Momenah Tarek S.,Gong Qiuming,Amin Ahmad S.,Ghamdi Saleh Al,Carvalho Julene S.,Homfray Tessa,Mannens Marcel M.A.M.,Zhou Zhengfeng,Wilde Arthur A.M.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference29 articles.

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2. Genetics of cardiac arrhythmias;Wilde;Heart,2005

3. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome;Curran;Cell,1995

4. Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia;Sanguinetti;Proc Natl Acad Sci U S A,1996

5. Cardiac IKr channels minimally comprise hERG 1a and 1b subunits;Jones;J Biol Chem,2004

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