RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa

Archives of Ophthalmology

Volumn 128, Issue 7, 2010, Pages 915-923

  Jayasundera, Thiran ^a   Branham, Kari E H ^a   Othman, Mohammad ^a   Rhoades, William R ^a   Karoukis, Athanasios J ^a   Khanna, Hemant ^a   Swaroop, Anand ^a,b   Heckenlively, John R ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHOROIDEREMIA; CLINICAL ARTICLE; DIFFERENTIAL DIAGNOSIS; ELECTRORETINOGRAPHY; EYE EXAMINATION; EYE FUNDUS; FEMALE; GENE MUTATION; GENETIC CORRELATION; GENETIC SCREENING; GENOTYPE; HETEROZYGOTE; HUMAN; MALE; MISSENSE MUTATION; MYOPIA; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINITIS PIGMENTOSA; SCHOOL CHILD; VISUAL ACUITY; VISUAL FIELD; X LINKED RETINITIS PIGMENTOSA;

ADOLESCENT; ADULT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; EYE PROTEINS; FEMALE; GENETIC DISEASES, X-LINKED; GENOTYPE; HETEROZYGOTE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PERIMETRY; PHENOTYPE; RETINITIS PIGMENTOSA; VISUAL ACUITY; VISUAL FIELDS;

EID: 77955006177     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2010.122     Document Type: Article

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