These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
222 related articles for article (PubMed ID: 17480003)
1. A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa. Banin E; Mizrahi-Meissonnier L; Neis R; Silverstein S; Magyar I; Abeliovich D; Roepman R; Berger W; Rosenberg T; Sharon D Am J Med Genet A; 2007 Jun; 143A(11):1150-8. PubMed ID: 17480003 [TBL] [Abstract][Full Text] [Related]
2. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60. Fishman GA; Grover S; Jacobson SG; Alexander KR; Derlacki DJ; Wu W; Buraczynska M; Swaroop A Ophthalmology; 1998 Dec; 105(12):2286-96. PubMed ID: 9855162 [TBL] [Abstract][Full Text] [Related]
3. Phenotype in two families with RP3 associated with RPGR mutations. Lorenz B; Andrassi M; Kretschmann U Ophthalmic Genet; 2003 Jun; 24(2):89-101. PubMed ID: 12789573 [TBL] [Abstract][Full Text] [Related]
4. X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa. Fahim AT; Sullivan LS; Bowne SJ; Jones KD; Wheaton DKH; Khan NW; Heckenlively JR; Jayasundera KT; Branham KH; Andrews CA; Othman MI; Karoukis AJ; Birch DG; Daiger SP Ophthalmol Retina; 2020 May; 4(5):510-520. PubMed ID: 31953110 [TBL] [Abstract][Full Text] [Related]
5. Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data. Wegscheider E; Preising MN; Lorenz B Graefes Arch Clin Exp Ophthalmol; 2004 Jun; 242(6):501-11. PubMed ID: 15173948 [TBL] [Abstract][Full Text] [Related]
6. Phenotypic high myopia in X-linked retinitis pigmentosa secondary to a novel mutation in the RPGR gene. Sanchez Tocino H; Diez Montero C; Villanueva Gómez A; Lobo Valentin R; Montero-Moreno JA Ophthalmic Genet; 2019 Apr; 40(2):170-176. PubMed ID: 31033374 [TBL] [Abstract][Full Text] [Related]
7. Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes. Andréasson S; Breuer DK; Eksandh L; Ponjavic V; Frennesson C; Hiriyanna S; Filippova E; Yashar BM; Swaroop A Ophthalmic Genet; 2003 Dec; 24(4):215-23. PubMed ID: 14566651 [TBL] [Abstract][Full Text] [Related]
8. Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa. Zhang Z; Dai H; Wang L; Tao T; Xu J; Sun X; Yang L; Li G BMC Ophthalmol; 2019 Nov; 19(1):240. PubMed ID: 31775781 [TBL] [Abstract][Full Text] [Related]
9. RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa. Sharon D; Sandberg MA; Rabe VW; Stillberger M; Dryja TP; Berson EL Am J Hum Genet; 2003 Nov; 73(5):1131-46. PubMed ID: 14564670 [TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics of high myopia in female carriers of pathogenic Tran M; Kolesnikova M; Kim AH; Kowal T; Ning K; Mahajan VB; Tsang SH; Sun Y Ophthalmic Genet; 2023 Jun; 44(3):295-303. PubMed ID: 36017691 [TBL] [Abstract][Full Text] [Related]
11. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa. Churchill JD; Bowne SJ; Sullivan LS; Lewis RA; Wheaton DK; Birch DG; Branham KE; Heckenlively JR; Daiger SP Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):1411-6. PubMed ID: 23372056 [TBL] [Abstract][Full Text] [Related]
12. Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations. Jin ZB; Liu XQ; Hayakawa M; Murakami A; Nao-i N Mol Vis; 2006 Oct; 12():1167-74. PubMed ID: 17093403 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family. Sheng X; Li Z; Zhang X; Wang J; Ren H; Sun Y; Meng R; Rong W; Zhuang W Mol Vis; 2010 Aug; 16():1620-8. PubMed ID: 20806050 [TBL] [Abstract][Full Text] [Related]
14. Visual Function in Carriers of X-Linked Retinitis Pigmentosa. Comander J; Weigel-DiFranco C; Sandberg MA; Berson EL Ophthalmology; 2015 Sep; 122(9):1899-906. PubMed ID: 26143542 [TBL] [Abstract][Full Text] [Related]
15. X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers. Kurata K; Hosono K; Hayashi T; Mizobuchi K; Katagiri S; Miyamichi D; Nishina S; Sato M; Azuma N; Nakano T; Hotta Y Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30917587 [TBL] [Abstract][Full Text] [Related]
16. X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15. Bader I; Brandau O; Achatz H; Apfelstedt-Sylla E; Hergersberg M; Lorenz B; Wissinger B; Wittwer B; Rudolph G; Meindl A; Meitinger T Invest Ophthalmol Vis Sci; 2003 Apr; 44(4):1458-63. PubMed ID: 12657579 [TBL] [Abstract][Full Text] [Related]
17. Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing. Neidhardt J; Glaus E; Lorenz B; Netzer C; Li Y; Schambeck M; Wittmer M; Feil S; Kirschner-Schwabe R; Rosenberg T; Cremers FP; Bergen AA; Barthelmes D; Baraki H; Schmid F; Tanner G; Fleischhauer J; Orth U; Becker C; Wegscheider E; Nürnberg G; Nürnberg P; Bolz HJ; Gal A; Berger W Mol Vis; 2008 Jun; 14():1081-93. PubMed ID: 18552978 [TBL] [Abstract][Full Text] [Related]
18. Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa. Zhao K; Wang L; Wang L; Wang L; Zhang Q; Wang Q Ophthalmic Genet; 2001 Sep; 22(3):187-94. PubMed ID: 11559860 [TBL] [Abstract][Full Text] [Related]
19. A novel mutation of the RPGR gene in a Chinese X-linked retinitis pigmentosa family and possible involvement of X-chromosome inactivation. Wang Y; Lu L; Zhang D; Tan Y; Li D; He F; Jiao X; Yang M; Hejtmancik JF; Liu X Eye (Lond); 2021 Jun; 35(6):1688-1696. PubMed ID: 32839555 [TBL] [Abstract][Full Text] [Related]
20. A population-based epidemiological and genetic study of X-linked retinitis pigmentosa. Prokisch H; Hartig M; Hellinger R; Meitinger T; Rosenberg T Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4012-8. PubMed ID: 17724181 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]