Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Long QT Syndrome and INA[original query] |
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Mutational analysis of SCN5A gene in long QT syndrome. Meta gene 2015 Dec 6 26-35. Qureshi Sameera Fatima, Ali Altaf, John Princy, Jadhav Amol P, Venkateshwari Ananthapur, Rao Hygriv, Jayakrishnan M P, Narasimhan Calambur, Shenthar Jayaprakash, Thangaraj Kumarasamy, Nallari Pratib |
Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Journal of the American Heart Association 2016 5 (7): . Veltmann Christian, Barajas-Martinez Hector, Wolpert Christian, Borggrefe Martin, Schimpf Rainer, Pfeiffer Ryan, Cáceres Gabriel, Burashnikov Elena, Antzelevitch Charles, Hu D |
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