Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

British Journal of Ophthalmology

Volumn 87, Issue 1, 2003, Pages 48-53

  Votruba, Marcela ^a,b   Thiselton, D ^a   Bhattacharya, S S ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CHROMOSOME 3Q; COLOR VISION; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GLAUCOMA; HEREDITARY OPTIC ATROPHY; HUMAN; INTRAOCULAR PRESSURE; MAJOR CLINICAL STUDY; MALE; MORPHOLOGY; OPTIC DISK; OPTIC NERVE; PRIORITY JOURNAL; PROSPECTIVE STUDY; RETINA MACULOPATHY; RETINOPATHY; VISUAL ACUITY; VISUAL FIELD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; GENOTYPE; GTP PHOSPHOHYDROLASES; HUMANS; LINKAGE (GENETICS); MALE; MUTATION; OPTIC ATROPHY, AUTOSOMAL DOMINANT; OPTIC DISK; PEDIGREE; PHENOTYPE; PHOTOGRAPHY; PROSPECTIVE STUDIES;

EID: 0037235396     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: 10.1136/bjo.87.1.48     Document Type: Article

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