A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Year: 2018
Type: article
Study design: Observational Study
Source: Genetics in Medicine
Authors: Claire Horvat, Renee Johnson, Lien Lam, Jacob Munro, Francesco Mazzarotto, Angharad M. Roberts, Daniel S. Herman, Michael Parfenov, Alireza Haghighi, Barbara McDonough, Steven R. DePalma, Anne M. Keogh, Peter S. Macdonald, Christopher S. Hayward, Amy Roberts, Paul J.R. Barton, Leanne E. Felkin, Eleni Giannoulatou, Stuart A. Cook, J.G. Seidman, Christine E. Seidman, Diane Fatkin
Institutions: Victor Chang Cardiac Research Institute, Howard Hughes Medical Institute, Harvard University, Royal Brompton & Harefield NHS Foundation Trust, NIHR Royal Brompton Cardiovascular Biomedical Research Unit, Imperial College London, Boston Children's Hospital, Brigham and Women's Hospital, UNSW Sydney, St Vincent's Hospital Sydney, National University of Singapore, National University Heart Centre Singapore, National Heart Centre Singapore
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Funders: Howard Hughes Medical Institute, Lee Foundation, National Institute for Health and Care Research, British Heart Foundation, Imperial College London, Harvard Club of Australia, Fondation Leducq, National Institutes of Health, Medical Research Council, National Health and Medical Research Council, National Heart, Lung, and Blood Institute
OpenAlex ID: W2808710939