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Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients

✍ Scribed by De-Kang Gan; Chen-Liang He; Hai-Rong Shu; Matthew R. Hoffman; Zi-Bing Jin

Book ID
116773422
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
501 KB
Volume
500
Category
Article
ISSN
0304-3940

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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