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Identification of a Kir3.4 mutation in congenital long QT syndrome.
Yang Y, Yang Y, Liang B, Liu J, Li J, Grunnet M, Olesen SP, Rasmussen HB, Ellinor PT, Gao L, Lin X, Li L, Wang L, Xiao J, Liu Y, Liu Y, Zhang S, Liang D, Peng L, Jespersen T, Chen YH. Yang Y, et al. Among authors: grunnet m. Am J Hum Genet. 2010 Jun 11;86(6):872-80. doi: 10.1016/j.ajhg.2010.04.017. Am J Hum Genet. 2010. PMID: 20560207 Free PMC article.
Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.
Calloe K, Ravn LS, Schmitt N, Sui JL, Duno M, Haunso S, Grunnet M, Svendsen JH, Olesen SP. Calloe K, et al. Among authors: grunnet m. Biochem Biophys Res Commun. 2007 Dec 28;364(4):889-95. doi: 10.1016/j.bbrc.2007.10.106. Epub 2007 Oct 29. Biochem Biophys Res Commun. 2007. PMID: 17967416
227 results