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Volumn 88, Issue 5, 1979, Pages 868-875
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A clinicopathologic study of autosomal dominant optic atrophy
a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
AUTOSOMAL DOMINANT INHERITANCE;
CASE REPORT;
CENTRAL NERVOUS SYSTEM;
COLOR VISION DEFECT;
ELECTRORETINOGRAPHY;
HEREDITY;
OPTIC NERVE ATROPHY;
PEDIGREE;
PERIPHERAL NERVOUS SYSTEM;
RETINA GANGLION CELL;
VISUAL ACUITY;
VISUAL SYSTEM;
ADULT;
CHILD;
COLOR VISION DEFECTS;
DEMYELINATING DISEASES;
ELECTRORETINOGRAPHY;
FEMALE;
GANGLIA;
GENES, DOMINANT;
HUMAN;
MALE;
MIDDLE AGE;
OPTIC ATROPHY;
OPTIC NERVE;
PEDIGREE;
RETINA;
SCOTOMA;
SUPPORT, U.S. GOV'T, P.H.S.;
VISUAL FIELDS;
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EID: 0018727407
PISSN: 00029394
EISSN: None
Source Type: Journal
DOI: 10.1016/0002-9394(79)90565-8 Document Type: Article |
Times cited : (153)
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References (23)
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