Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Shock and SCN5A[original query] |
---|
SCN5A mutation is associated with early and frequent recurrence of ventricular fibrillation in patients with Brugada syndrome. Circulation journal : official journal of the Japanese Circulation Society 2010 Nov 74 (12): 2572-8. Nishii Nobuhiro, Ogawa Masahiro, Morita Hiroshi, Nakamura Kazufumi, Banba Kimikazu, Miura Daiji, Kumagai Naoko, Matsunaga Akira, Kawamura Hiroshi, Urakawa Shigemi, Miyaji Kohei, Nagai Masahiro, Satoh Katsumasa, Nakagawa Koji, Tanaka Masamichi, Hiramatsu Shigeki, Tada Takeshi, Murakami Masato, Nagase Satoshi, Kohno Kunihisa, Kusano Kengo Fukushima, Saku Keijiro, Ohe Tohru, Ito Hiros |
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction. Circulation. Cardiovascular genetics 2011 Apr 4 (2): 163-8. Sun Albert Y, Koontz Jason I, Shah Svati H, Piccini Jonathan P, Nilsson Kent R, Craig Damian, Haynes Carol, Gregory Simon G, Hranitzky Patrick M, Pitt Geoffrey |
Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2018 5 23 (5): e12548. Robyns Tomas, Nuyens Dieter, Vandenberk Bert, Kuiperi Cuno, Corveleyn Anniek, Breckpot Jeroen, Garweg Christophe, Ector Joris, Willems R |
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype. Frontiers in genetics 2019 6 10 547. Micaglio Emanuele, Monasky Michelle M, Ciconte Giuseppe, Vicedomini Gabriele, Conti Manuel, Mecarocci Valerio, Giannelli Luigi, Giordano Federica, Pollina Alberto, Saviano Massimo, Pozzi Paolo R, Di Resta Chiara, Benedetti Sara, Ferrari Maurizio, Santinelli Vincenzo, Pappone Car |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: