Similar articles for PMID: 14564670

Year	Number of Results
1997	5
1998	4
1999	5
2000	3
2001	4
2002	8
2003	6
2004	1
2005	9
2006	9
2007	10
2008	6
2009	6
2010	9
2011	10
2012	11
2013	9
2014	12
2015	12
2016	10
2017	6
2018	11
2019	11
2020	26
2021	22
2022	19
2023	10
2024	0

1

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. Sharon D, et al. Am J Hum Genet. 2003 Nov;73(5):1131-46. doi: 10.1086/379379. Epub 2003 Oct 16. Am J Hum Genet. 2003. PMID: 14564670 Free PMC article.

2

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. Andréasson S, et al. Ophthalmic Genet. 2003 Dec;24(4):215-23. doi: 10.1076/opge.24.4.215.17228. Ophthalmic Genet. 2003. PMID: 14566651

3

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. Bader I, et al. Invest Ophthalmol Vis Sci. 2003 Apr;44(4):1458-63. doi: 10.1167/iovs.02-0605. Invest Ophthalmol Vis Sci. 2003. PMID: 12657579

4

Visual Function in Carriers of X-Linked Retinitis Pigmentosa.

Comander J, Weigel-DiFranco C, Sandberg MA, Berson EL. Comander J, et al. Ophthalmology. 2015 Sep;122(9):1899-906. doi: 10.1016/j.ophtha.2015.05.039. Epub 2015 Jul 2. Ophthalmology. 2015. PMID: 26143542 Free PMC article.

5

X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.

Sharon D, Bruns GA, McGee TL, Sandberg MA, Berson EL, Dryja TP. Sharon D, et al. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2712-21. Invest Ophthalmol Vis Sci. 2000. PMID: 10937588

6

Mutations in RPGR and RP2 of Chinese patients with X-linked retinitis pigmentosa.

Ji Y, Wang J, Xiao X, Li S, Guo X, Zhang Q. Ji Y, et al. Curr Eye Res. 2010 Jan;35(1):73-9. doi: 10.3109/02713680903395299. Curr Eye Res. 2010. PMID: 20021257

7

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. Jin ZB, et al. Mol Vis. 2006 Oct 6;12:1167-74. Mol Vis. 2006. PMID: 17093403 Free article.

8

Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.

Jin ZB, Gu F, Ma X, Nao-i N. Jin ZB, et al. Arch Ophthalmol. 2007 Oct;125(10):1407-12. doi: 10.1001/archopht.125.10.1407. Arch Ophthalmol. 2007. PMID: 17923551

9

Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 Years.

Cideciyan AV, Charng J, Roman AJ, Sheplock R, Garafalo AV, Heon E, Jacobson SG. Cideciyan AV, et al. Invest Ophthalmol Vis Sci. 2018 Sep 4;59(11):4558-4566. doi: 10.1167/iovs.18-24931. Invest Ophthalmol Vis Sci. 2018. PMID: 30208424

10

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.

Breuer DK, Yashar BM, Filippova E, Hiriyanna S, Lyons RH, Mears AJ, Asaye B, Acar C, Vervoort R, Wright AF, Musarella MA, Wheeler P, MacDonald I, Iannaccone A, Birch D, Hoffman DR, Fishman GA, Heckenlively JR, Jacobson SG, Sieving PA, Swaroop A. Breuer DK, et al. Am J Hum Genet. 2002 Jun;70(6):1545-54. doi: 10.1086/340848. Epub 2002 Apr 30. Am J Hum Genet. 2002. PMID: 11992260 Free PMC article.

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