Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation

Archives of Ophthalmology

Volumn 118, Issue 9, 2000, Pages 1269-1276

  Oh, Kean T ^a   Weleber, Richard G ^b,c   Lotery, Andrew ^a   Oh, Dawn M ^a   Billingslea, Andrea M ^b   Stone, Edwin M ^a  

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

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; HISTIDINE; PROLINE; RHODOPSIN;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; CLINICAL FEATURE; CODON; ELECTRORETINOGRAM; FEMALE; GENE MUTATION; HUMAN; MALE; NIGHT BLINDNESS; ONSET AGE; PHENOTYPE; PHOTOPHOBIA; PRIORITY JOURNAL; RETINA MALFORMATION; RETINITIS PIGMENTOSA; VISUAL FIELD;

EID: 0033817044     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.118.9.1269     Document Type: Article

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