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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: sanatani s. Genet Med. 2008 Jul;10(7):545-50. doi: 10.1097/gim.0b013e31817c6b19. Genet Med. 2008. PMID: 18580685
Catecholaminergic polymorphic ventricular tachycardia in children: analysis of therapeutic strategies and outcomes from an international multicenter registry.
Roston TM, Vinocur JM, Maginot KR, Mohammed S, Salerno JC, Etheridge SP, Cohen M, Hamilton RM, Pflaumer A, Kanter RJ, Potts JE, LaPage MJ, Collins KK, Gebauer RA, Temple JD, Batra AS, Erickson C, Miszczak-Knecht M, Kubuš P, Bar-Cohen Y, Kantoch M, Thomas VC, Hessling G, Anderson C, Young ML, Cabrera Ortega M, Lau YR, Johnsrude CL, Fournier A, Kannankeril PJ, Sanatani S. Roston TM, et al. Among authors: sanatani s. Circ Arrhythm Electrophysiol. 2015 Jun;8(3):633-42. doi: 10.1161/CIRCEP.114.002217. Epub 2015 Feb 24. Circ Arrhythm Electrophysiol. 2015. PMID: 25713214 Free PMC article.
243 results