Work

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

Year: 2000

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/9.5.795

Authors: M. Jaksch, I Ogilvie, J Yao, G Kortenhaus, H G Bresser, K D Gerbitz, E A Shoubridge

Institutions: München Klinik Schwabing, Institute of Diabetes Research

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2152585412

FWCI: 5.081

Cites: 32

Cited by: 223

Related to: 10