Refinement of the locus for autosomal dominant juvenile optic atrophy to a 2 cM region on 3q28

Ophthalmic Genetics

Volumn 18, Issue 1, 1997, Pages 1-6

  Stoilova, D ^a   Child, A ^a   Desai, S P ^a   Sarfarazi, M ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

Chromosome 3q28; Fine mapping; Juvenile optic atrophy (Kjer type)

Indexed keywords

DNA MARKER;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 3Q; CLINICAL ARTICLE; COLOR VISION; CONTROLLED STUDY; DNA FLANKING REGION; FAMILY; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENETIC RECOMBINATION; GENOTYPE; HAPLOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; MALE; MOLECULAR CLONING; PRIORITY JOURNAL; VISUAL ACUITY; VISUAL DISORDER; VISUAL FIELD;

EID: 0030918368     PISSN: 01676784     EISSN: None     Source Type: Journal    
DOI: 10.3109/13816819709057877     Document Type: Article

References (14)