Leber's hereditary optic neuropathy: A model for mitochondrial neurodegenerative diseases

FASEB Journal

Volumn 6, Issue 10, 1992, Pages 2791-2799

  Brown, M D ^a   Voljavec, A S ^a   Lott, M T ^a   MacDonald, I ^a   Wallace, D C ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

genotype; Leber's hereditary optic neuropathy; mitochondrial DNA mutations; oxidative phosphorylation

Indexed keywords

MITOCHONDRIAL DNA;

DISEASE CLASSIFICATION; DISEASE MODEL; GENOME; GENOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; NERVE DEGENERATION; PEDIGREE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; REVIEW;

EID: 0026702249     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fasebj.6.10.1634041     Document Type: Review

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