✦ LIBER ✦

290 The KCNQ1 rs2074238 polymorphism is a genetic modifier of cardiac risk in long QT syndrome

✍ Scribed by Duchatelet, Sabine; Peat, Rachel; Denjoy, Isabelle; Itoh, Hideki; Berthet, Myriam; Crotti, Lia; Ohno, Seiko; Fressart, Véronique; Pedrazzini, Matteo; Klug, Didier; Trégouët, David-Alexandre; Schwartz, Peter J.; Shimizu, Wataru; Horie, Minoru; Guicheney, Pascale

Book ID: 119641964
Publisher: Elsevier
Year: 2012
Tongue: English
Weight: 63 KB
Volume: 4
Category: Article
ISSN: 1878-6480
DOI: 10.1016/s1878-6480(12)70686-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations in Conserved Amino Acids in th

Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome

✍ CHRISTIAN JONS; ARTHUR J. MOSS; COELI M. LOPES; SCOTT MCNITT; WOJCIECH ZAREBA; I 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 756 KB

Single nucleotide polymorphisms in arrhy

Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome

✍ Earle, Nikki; Yeo Han, Dug; Pilbrow, Anna; Crawford, Jackie; Smith, Warren; Shel 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 232 KB

Neural Control of Heart Rate Is an Arrhy

Neural Control of Heart Rate Is an Arrhythmia Risk Modifier in Long QT Syndrome

✍ Peter J. Schwartz; Emilio Vanoli; Lia Crotti; Carla Spazzolini; Chiara Ferrandi; 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 639 KB

Ion Channel Mechanisms Related to Sudden

Ion Channel Mechanisms Related to Sudden Cardiac Death in Phenotype-Negative Long-QT Syndrome Genotype–Phenotype Correlations of the KCNQ1(S349W) Mutation

✍ SAMUEL HORR; ILAN GOLDENBERG; ARTHUR J. MOSS; JIN O-UCHI; ALON BARSHESHET; HEATH 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 458 KB

Genotype-specific QT correction for hear

Genotype-specific QT correction for heart rate and the risk of life-threatening cardiac events in adolescents with congenital long-QT syndrome

✍ Barsheshet, Alon; Peterson, Derick R.; Moss, Arthur J.; Schwartz, Peter J.; Kauf 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 455 KB

The −974C>A (rs3087459) gene polymorphis

The −974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients

✍ Vargas-Alarcon, Gilberto; Vallejo, Maite; Posadas-Romero, Carlos; Juarez-Rojas, 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 293 KB