The genetic basis of Brugada syndrome: A mutation update-Reference-Cited by-同舟云学术

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The genetic basis of Brugada syndrome: A mutation update

Published:2009-09 Issue:9 Volume:30 Page:1256-1266
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Hedley Paula L.,JÃ¸rgensen Poul,Schlamowitz Sarah,Moolman-Smook Johanna,Kanters JÃ¸rgen K.,Corfield Valerie A.,Christiansen Michael

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21066/fullpdf

Reference175 articles.

1. MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis;Abbott;Cell,2001

2. Do all voltage-gated potassium channels use MiRPs?;Abbott;Circ Res,2001

3. Disease-associated mutations in KCNE potassium channel subunits (MiRPs) reveal promiscuous disruption of multiple currents and conservation of mechanism;Abbott;FASEB J,2002

4. MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia;Abbott;Cell,1999

5. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing;Ackerman;Heart Rhythm,2004

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