Work

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

Year: 2000

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/9.8.1245

Authors: I. Valnot, J C von Kleist-Retzow, A Barrientos, M Gorbatyuk, J W Taanman, B Mehaye, P Rustin, A Tzagoloff, A Munnich, A Rötig

Institutions: Hôpital Necker-Enfants Malades, Inserm, Université Paris Descartes

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

Funder: National Institute of General Medical Sciences

Award: Heme A and cytochrome oxidase biosynthesis

OpenAlex ID: W2111375801

FWCI: 6.967

Cites: 31

Cited by: 303

Related to: 10