X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR

Archives of Ophthalmology

Volumn 115, Issue 11, 1997, Pages 1429-1435

  Weleber, Richard G ^a,c   Butler, Noah S ^b   Murphey, William H ^b   Sheffield, Val C ^b   Stone, Edwin M ^b  

^a Departments of Ophthalmology

^b UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

^c CASEY EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BASE PAIRING; CLINICAL ARTICLE; CODON; ELECTRORETINOGRAPHY; FAMILY; FEMALE; FLUORESCENCE ANGIOGRAPHY; FRAMESHIFT MUTATION; GENE INSERTION; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; PERIMETRY; PHENOTYPE; PRIORITY JOURNAL; RETINA CONE; RETINITIS PIGMENTOSA; VISUAL FIELD DEFECT; X CHROMOSOME LINKED DISORDER;

EID: 0031468640     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.1997.01100160599013     Document Type: Article

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