Work

Cardiomyopathy and carnitine deficiency

Year: 2008

Type: article

Study design: Observational Study

Source: Molecular Genetics and Metabolism

DOI: 10.1016/j.ymgme.2008.02.002

Authors: Cristina Amat di San Filippo, Matthew R.G. Taylor, Luisa Mestroni, Lorenzo D. Botto, Nicola Longo

Institutions: University of Utah, University of Colorado Denver

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: American Heart Association, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Advancing Translational Sciences

Awards: G1682441725, THE CARNITINE TRANSPORTER IN HUMAN DISEASE, G4567733944, Colorado Clinical and Translational Sciences Institute, Familial Dilated Cardiomyopathy:Genetic Characterization

OpenAlex ID: W2095664992

FWCI: 5.09

Cites: 28

Cited by: 72

Related to: 10