Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His

American Journal of Ophthalmology

Volumn 134, Issue 2, 2002, Pages 290-293

  To, King ^a   Adamian, Michael ^a   Dryja, Thaddeus P ^a   Berson, Eliot L ^a,b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HISTIDINE; PROLINE; RHODOPSIN;

AGED; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; ELECTRON MICROSCOPY; FEMALE; GENE MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MICROSCOPY; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA DEGENERATION; RETINITIS PIGMENTOSA;

EID: 0036327111     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(02)01545-3     Document Type: Article

References (5)

1. Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa
2. Histopathology of bone spicule pigmentation in retinitis pigmentosa
3. Autosomal dominant sectoral retinitis pigmentosa: Two families with transversion mutation in codon 23 of rhodopsin
4. Regional distribution of retinal degeneration in patients with proline to histidine mutation in codon 23 of the rhodopsin gene
5. Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro23His)