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A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact.
Arbour L, Rezazadeh S, Eldstrom J, Weget-Simms G, Rupps R, Dyer Z, Tibbits G, Accili E, Casey B, Kmetic A, Sanatani S, Fedida D. Arbour L, et al. Among authors: tibbits g. Genet Med. 2008 Jul;10(7):545-50. doi: 10.1097/gim.0b013e31817c6b19. Genet Med. 2008. PMID: 18580685
In vitro analyses of suspected arrhythmogenic thin filament variants as a cause of sudden cardiac death in infants.
Shafaattalab S, Li AY, Lin E, Stevens CM, Dewar LJ, Lynn FC, Sanatani S, Laksman Z, Morin RD, van Petegem F, Hove-Madsen L, Tieleman DP, Davis JP, Tibbits GF. Shafaattalab S, et al. Proc Natl Acad Sci U S A. 2019 Apr 2;116(14):6969-6974. doi: 10.1073/pnas.1819023116. Epub 2019 Mar 18. Proc Natl Acad Sci U S A. 2019. PMID: 30886088 Free PMC article.
120 results