PubMed

Rhodopsin mutations in Chinese patients with retinitis pigmentosa.

Chan WM, Yeung KY, Pang CP, Baum L, Lau TC, Kwok AK, Lam DS.

Br J Ophthalmol. 2001 Sep;85(9):1046-8.PMID: 11520753 [PubMed - indexed for MEDLINE]Related articlesFree article

[Screening for point mutations in rhodopsin gene among one hundred Chinese patients with retinitis pigmentosa]

Zhang X, Fu W, Pang CP, Yeung KY.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Dec;19(6):463-6. Chinese. PMID: 12476415 [PubMed - indexed for MEDLINE]Related articles

A complete screen for mutations of the rhodopsin gene in a panel of Chinese patients with autosomal dominant retinitis pigmentosa.

Zhang XL, Liu M, Meng XH, Fu WL, Yin ZQ, Zhang X, Huang JF.

Chin Med Sci J. 2005 Mar;20(1):30-4.PMID: 15844309 [PubMed - indexed for MEDLINE]Related articles

[Digenic association of RHO and RP1 genes with retinitis pigmentosa among Chinese population in Hong Kong]

Wang DY, Fan BJ, Chan WM, Tam OS, Chiang WY, Lam SC, Pang CP.

Zhonghua Yi Xue Za Zhi. 2005 Jun 22;85(23):1613-7. Chinese. PMID: 16185528 [PubMed - indexed for MEDLINE]Related articles

Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

Zhao K, Xiong S, Wang L, Wang L, Cui Y, Wang Q.

Ophthalmic Genet. 2001 Sep;22(3):155-62.PMID: 11559857 [PubMed - indexed for MEDLINE]Related articles

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

Dryja TP, McGee TL, Hahn LB, Cowley GS, Olsson JE, Reichel E, Sandberg MA, Berson EL.

N Engl J Med. 1990 Nov 8;323(19):1302-7.PMID: 2215617 [PubMed - indexed for MEDLINE]Related articles

[Mutation analysis of retinitis pigmentosa 1 gene in Chinese with retinitis pigmentosa]

Zhang X, Yeung KY, Pang CP, Fu W.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Jun;19(3):194-7. Chinese. PMID: 12048676 [PubMed - indexed for MEDLINE]Related articles

Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4.

Bareil C, Hamel C, Pallarès-Ruiz N, Arnaud B, Demaille J, Claustres M.

Ophthalmic Genet. 1999 Sep;20(3):173-82.PMID: 10521250 [PubMed - indexed for MEDLINE]Related articles

[Analysis of rhodopsin and peripherin/RDS genes in Chinese patients with retinitis pigmentosa]

Zhang F, Zhang Q, Shen H, Li S, Xiao X.

Yan Ke Xue Bao. 1998 Dec;14(4):210-4. Chinese. PMID: 12579739 [PubMed - indexed for MEDLINE]Related articles

Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).

Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP.

Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2217-24.PMID: 11527933 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosa.

Lim KP, Yip SP, Cheung SC, Leung KW, Lam ST, To CH.

Arch Ophthalmol. 2009 Jun;127(6):784-90.PMID: 19506198 [PubMed - indexed for MEDLINE]Related articles

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.

Schuster A, Weisschuh N, Jägle H, Besch D, Janecke AR, Zierler H, Tippmann S, Zrenner E, Wissinger B.

Br J Ophthalmol. 2005 Oct;89(10):1258-64.PMID: 16170112 [PubMed - indexed for MEDLINE]Related articlesFree article

Screening for mutations in a novel retinal-specific gene among Chinese patients with retinitis pigmentosa.

Xiaoli Z, Weiling F, Pang CP, Yeung KY.

Chin Med Sci J. 2002 Dec;17(4):225-30.PMID: 12901510 [PubMed - indexed for MEDLINE]Related articles

Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa.

Fujiki K, Hotta Y, Murakami A, Yoshii M, Hayakawa M, Ichikawa T, Takeda M, Akeo K, Okisaka S, Kanai A.

Jpn J Hum Genet. 1995 Sep;40(3):271-7.PMID: 8527802 [PubMed - indexed for MEDLINE]Related articles

RP1 in Chinese: Eight novel variants and evidence that truncation of the extreme C-terminal does not cause retinitis pigmentosa.

Baum L, Chan WM, Yeung KY, Lam DS, Kwok AK, Pang CP.

Hum Mutat. 2001 May;17(5):436.PMID: 11317367 [PubMed - indexed for MEDLINE]Related articles

A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease.

Sullivan LJ, Makris GS, Dickinson P, Mulhall LE, Forrest S, Cotton RG, Loughnan MS.

Arch Ophthalmol. 1993 Nov;111(11):1512-7.PMID: 8240107 [PubMed - indexed for MEDLINE]Related articles

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Dryja TP, McGee TL, Reichel E, Hahn LB, Cowley GS, Yandell DW, Sandberg MA, Berson EL.

Nature. 1990 Jan 25;343(6256):364-6.PMID: 2137202 [PubMed - indexed for MEDLINE]Related articles

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

Inglehearn CF, Keen TJ, Bashir R, Jay M, Fitzke F, Bird AC, Crombie A, Bhattacharya S.

Hum Mol Genet. 1992 Apr;1(1):41-5.PMID: 1301135 [PubMed - indexed for MEDLINE]Related articles

Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.

DeAngelis MM, Grimsby JL, Sandberg MA, Berson EL, Dryja TP.

Arch Ophthalmol. 2002 Mar;120(3):369-75.PMID: 11879142 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.

Dryja TP, Hahn LB, Cowley GS, McGee TL, Berson EL.

Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9370-4.PMID: 1833777 [PubMed - indexed for MEDLINE]Related articlesFree article