Work

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy

Year: 1997

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.49.4.1136

Authors: V. Biousse, M. D. Brown, N. J. Newman, J. C. Allen, J. Rosenfeld, G. Meola, D. C. Wallace

Institutions: Emory University, University of Milan, IRCCS Policlinico San Donato

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 Eye Institute, National Institute of Neurological Disorders and Stroke

Awards: G2718742063, G3606576165, COMPLEX I DYSFUNCTION IN LEBER'S OPTIC ATROPHY, Mitochondrial Inborn Errors in Metabolism

OpenAlex ID: W2004878132

FWCI: 0.707

Cites: 4

Cited by: 62

Related to: 10