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hERG long QT syndrome type 2 mutants need more than a chaperone to dance
Author(s) -
Fedida David,
Macdonald Logan
Publication year - 2016
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp272417
Subject(s) - herg , long qt syndrome , qt interval , medicine , nonsense mutation , missense mutation , brugada syndrome , sudden death , potassium channel , short qt syndrome , repolarization , cardiac action potential , pharmacology , mutation , genetics , biology , gene , electrophysiology