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Non-allelic mutations in X-linked retinitis pigmentosa

✍ Scribed by J. D. Chen; P. Dickinson; R. Gray; I. Constable; L. Sheffield; M. J. Denton

Book ID
115089893
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
279 KB
Volume
35
Category
Article
ISSN
0009-9163

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X-linked forms of retinitis pigmentosa (XLRP) are among the most severe because of their early onset, often leading to significant visual impairment before the fourth decade. RP3, genetically localized at Xp21.1, accounts for 70% of XLRP in different populations. The RPGR (Retinitis Pigmentosa GTPas