Work

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Year: 1995

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng1295-438

Authors: Gisèle Bonne, Lucie Carrier, Josiane Bercovici, Corinne Cruaud, Pascale Richard, Bernard Hainque, Mathias Gautel, Siegfried Labeit, Michael James, Jacques Beckmann, Jean Weissenbach, Hans-Peter Vosberg, Marc Fiszman, Michel Komajda, Ketty Schwartz

Institutions: Inserm, Pitié-Salpêtrière Hospital, Centre National de la Recherche Scientifique, European Molecular Biology Laboratory, Centre for Human Genetics, Max Planck Society

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: W2070163453

FWCI: 25.54

Cites: 28

Cited by: 436

Related to: 10