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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 15, 2025. (Total: 235337Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Brugada Syndrome and CACNA2D1[original query]
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Dec 7 (12): 1872-82.
Burashnikov Elena, Pfeiffer Ryan, Barajas-Martinez Héctor, Delpón Eva, Hu Dan, Desai Mayurika, Borggrefe Martin, Häissaguerre Michel, Kanter Ronald, Pollevick Guido D, Guerchicoff Alejandra, Laiño Ruben, Marieb Mark, Nademanee Koonlawee, Nam Gi-Byoung, Robles Roberto, Schimpf Rainer, Stapleton Dwight D, Viskin Sami, Winters Stephen, Wolpert Christian, Zimmern Samuel, Veltmann Christian, Antzelevitch Charl
High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.
Clinical genetics 2013 Nov 84 (5): 489-95.
Risgaard B, Jabbari R, Refsgaard L, Holst A G, Haunsø S, Sadjadieh A, Winkel B G, Olesen M S, Tfelt-Hansen
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation.
Scientific reports 2018 10 8 (1): 14619.
Blancard Malorie, Debbiche Amal, Kato Koichi, Cardin Christelle, Sabrina Guichard, Gandjbakhch Estelle, Probst Vincent, Haissaguerre Michel, Extramiana Fabrice, Hocini Mélèze, Olivier Geoffroy, Leenhardt Antoine, Guicheney Pascale, Rougier Jean-Sébasti
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