A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology

American Journal of Human Genetics

Volumn 51, Issue 6, 1992, Pages 1218-1228

  Mackey, D ^a   Howell, N ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; CLINICAL ARTICLE; EXTRACHROMOSOMAL INHERITANCE; GENE MUTATION; GENEALOGY; HEREDITARY OPTIC ATROPHY; HUMAN; MITOCHONDRION; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; RISK ASSESSMENT; VISION; VISUAL ACUITY; VISUAL FIELD DEFECT;

ADOLESCENT; ADULT; CHILD; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; FEMALE; HUMAN; MALE; MIDDLE AGE; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; VISUAL ACUITY;

EID: 0026746739     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)