Work

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

Year: 1995

Type: article

Study design: Observational Study

Source: Brain

DOI: 10.1093/brain/118.2.319

Authors: P. Riordan-Eva, M. D. Sanders, G. G. Govan, M. G. Sweeney, J. Da Costa, A. E. Harding

Institutions: National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology

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: Wellcome Trust

OpenAlex ID: W2070864958

FWCI: 6.017

Cites:

Cited by: 491

Related to: 10