Work

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Year: 1994

Type: article

Study design: Observational Study

Source: Cell

DOI: 10.1016/0092-8674(94)90054-x

Authors: Ludwig Thierfelder, Hugh Watkins, Calum MacRae, Roger Lamas, William McKenna, Hans-Peter Vosberg, J.G. Seldman, Christine E. Seidman

Institutions: Brigham and Women's Hospital, Howard Hughes Medical Institute, Harvard University, St George's, University of London, Hospital Militar de Santiago, 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

Funders: Wellcome Trust, National Heart, Lung, and Blood Institute

Awards: GENETIC ANALYSIS OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, MOLECULAR CAUSE OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

OpenAlex ID: W1995697852

FWCI: 51.56

Cites: 49

Cited by: 1,040

Related to: 10