Clinical course and visual function in a family with mutations in the RPE65 gene

Archives of Ophthalmology

Volumn 120, Issue 1, 2002, Pages 55-61

  Felius, Joost ^a   Thompson, Debra A ^a   Khan, Naheed W ^a   Bingham, Eve L ^a   Jamison, Jeffrey A ^a   Kemp, Jennifer A ^a   Sieving, Paul A ^a,b  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b NATIONAL EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; COLOR VISION; CONTRAST SENSITIVITY; DRUSEN; ELECTRORETINOGRAPHY; EYE FUNDUS; FEMALE; GENE MUTATION; GENETIC SCREENING; HETEROZYGOTE; HUMAN; MALE; MISSENSE MUTATION; NULL ALLELE; PERIMETRY; PHENOTYPE; PHOTORECEPTOR; PHOTOTRANSDUCTION; PIGMENT EPITHELIUM; PRIORITY JOURNAL; VISION; VISION TEST; VISUAL ACUITY; VISUAL FIELD; VISUAL IMPAIRMENT;

EID: 0036295099     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.120.1.55     Document Type: Article

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