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Volumn 2, Issue 5, 2000, Pages 283-289
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Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families
a,c a,c a,c d b a,c d a,c
d
NONE
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Author keywords
Chromosome 3q; Dominant; Linkage; Optic atrophy; Sex influenced variation
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Indexed keywords
ADOLESCENT;
ADULT;
AGE;
AGED;
ARTICLE;
AUTOSOMAL DOMINANT INHERITANCE;
CHROMOSOME 3Q;
CLINICAL ARTICLE;
COLOR VISION;
FAMILIAL INCIDENCE;
FEMALE;
GENETIC HETEROGENEITY;
GENETIC LINKAGE;
HEREDITARY OPTIC ATROPHY;
HUMAN;
MALE;
POPULATION RESEARCH;
RISK FACTOR;
SEX DIFFERENCE;
VISUAL IMPAIRMENT;
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EID: 0033767526
PISSN: 10983600
EISSN: None
Source Type: Journal
DOI: 10.1097/00125817-200009000-00003 Document Type: Article |
Times cited : (7)
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References (24)
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