Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function.
Li W, Wang QF, Du R, Xu QM, Ke QM, Wang B, Chen XL, Tian L, Zhang SY, Kang CL, Guan SM, Yang JG, Song ZF.
Li W, et al.
Biochem Biophys Res Commun. 2009 Feb 27;380(1):127-31. doi: 10.1016/j.bbrc.2009.01.051. Epub 2009 Jan 22.
Biochem Biophys Res Commun. 2009.
PMID: 19167356