Work

Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

Year: 1995

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng1295-434

Authors: Hugh Watkins, David Conner, Ludwig Thierfelder, John A. Jarcho, Calum MacRae, William J. McKenna, Barry J. Maron, J.G. Seidman, Christine E. Seidman

Institutions: Brigham and Women's Hospital, St George's Hospital, Howard Hughes Medical Institute, St George's, University of London, Harvard University, Max Delbrück Center, Minneapolis Heart Institute Foundation

Language: English

Topic: Cardiomyopathy and Myosin Studies

Subfield: Cardiology and Cardiovascular Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Wellcome Trust

OpenAlex ID: W2034972644

FWCI: 29.79

Cites: 22

Cited by: 584

Related to: 10