Work

An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblasts

Year: 1991

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.41.12.1957

Authors: R. Lutz, A. Garnica, A. Shires, E. Freneaux, D. De Vivo, P. Neuhoff, W. J. Rhead

Institutions: University of Iowa, Columbia University Irving Medical Center, University of Oklahoma Health Sciences Center, University of Oklahoma

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

Funders: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G3147062916, INHERITED DISORDERS OF OXIDATIVE METABOLISM IN MAN

OpenAlex ID: W2107643478

FWCI:

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