Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Bradycardia and HCN4[original query] |
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HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy. European journal of medical genetics 2015 Sep 58 (9): 439-42. Millat Gilles, Janin Alexandre, de Tauriac Olivier, Roux Antoine, Dauphin Clai |
A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotype. Revista espanola de cardiologia (English ed.) 2020 10 74 (9): 781-789. Alonso-Fernández-Gatta Marta, Gallego-Delgado María, Caballero Ricardo, Villacorta Eduardo, Díaz-Peláez Elena, García-BerrocaL Belén, Crespo-García Teresa, Plata-Izquierdo Beatriz, Marcos-Vadillo Elena, García-Cuenllas Luisa, Barreiro-Pérez Manuel, Isidoro-García María, Tamargo-Menéndez Juan, Delpón Eva, Sánchez Pedro |
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of Noncompaction. Journal of cardiac failure 2021 6 27 (6): 677-681. Cambon-Viala Marie, Gerard Hilla, Nguyen Karine, Richard Pascale, Ader Flavie, Pruny Jean-François, Donal Erwan, Eicher Jean-Christophe, Huttin Olivier, Selton-Suty Christine, Raud-Raynier Pascale, Jondeau Guillaume, Mansencal Nicolas, Sawka Caroline, Casalta Anne-Claire, Michel Nicolas, Donghi Valeria, Martel Hélène, Faivre Laurence, Charron Philippe, Habib Gilbe |
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