Kv7.1 (KCNQ1) properties and channelopathies
Author:
Publisher
Wiley
Subject
Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/jphysiol.2007.148254/fullpdf
Reference21 articles.
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2. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.;Bellocq;Circulation,2004
3. In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.;Bendahhou;Cardiovasc Res,2005
4. Phosphatidylinositol 4,5-bisphosphate interactions with the HERG K+ channel.;Bian;Pflugers Arch,2007
5. KCNQ1 gain-of-function mutation in familial atrial fibrillation.;Chen;Science,2003
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