Year: 2016
Type: article
Study design: Observational Study
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: European Commission, Fondation Leducq, National Institutes of Health, National Heart, Lung, and Blood Institute, National Center for Research Resources, National Center for Advancing Translational Sciences, Colorado Clinical and Translational Sciences Institute, FP7 People: Marie-Curie Actions
Awards: G1210576399, G1825981810, Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy, G1918775905, G252781271, G2594075514, G2899602109, G319511802, G3665166657, G3793127575, G3876424838, G4102444154, G4146012505, G4531593092, G4921130661, Molecular Genetics, Pathogenesis and Protein-Replacement Therapy in Arrhythmogenic Cardiomyopathy, Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathy, G5366298750, G5535094332, Colorado Clinical and Translational Sciences Institute, G6300707817, G70312321, Sarcomere based Signals in Muscle Remodelling, G7466124990, G8694940605, Molecular Epidemiology of Dilated Cardiomyopath, G9000060836, Colorado Clinical and Translational Science Institute (UL1)
OpenAlex ID: W2551477390
