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.
136 related articles for article (PubMed ID: 9070228)
1. Identification of a polymorphic missense (G338D) and silent (106V and 121L) mutations within the coding region of the peripherin/RDS gene in a patient with retinitis punctata albescens. Shastry BS; Trese MT Biochem Biophys Res Commun; 1997 Feb; 231(1):103-5. PubMed ID: 9070228 [TBL] [Abstract][Full Text] [Related]
2. Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene. Souied E; Soubrane G; Benlian P; Coscas GJ; Gerber S; Munnich A; Kaplan J Am J Ophthalmol; 1996 Jan; 121(1):19-25. PubMed ID: 8554077 [TBL] [Abstract][Full Text] [Related]
3. Two novel missense mutations in the peripherin/RDS gene in two unrelated French patients with autosomal dominant retinitis pigmentosa. Souied EH; Rozet JM; Gerber S; Dufier JL; Soubrane G; Coscas G; Munnich A; Kaplan J Eur J Ophthalmol; 1998; 8(2):98-101. PubMed ID: 9673478 [TBL] [Abstract][Full Text] [Related]
4. Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system. Ekström U; Ponjavic V; Andréasson S; Ehinger B; Nilsson-Ehle P; Abrahamson M Mol Pathol; 1998 Oct; 51(5):287-91. PubMed ID: 10193525 [TBL] [Abstract][Full Text] [Related]
5. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens. Kajiwara K; Sandberg MA; Berson EL; Dryja TP Nat Genet; 1993 Mar; 3(3):208-12. PubMed ID: 8485575 [TBL] [Abstract][Full Text] [Related]
6. Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa. Dryja TP; Hahn LB; Kajiwara K; Berson EL Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1972-82. PubMed ID: 9331261 [TBL] [Abstract][Full Text] [Related]
7. Peripherin/RDS gene mutation (Pro210Leu) and polymorphisms in Japanese patients with retinal dystrophies. Budu ; Hayasaka S; Matsumoto M; Yamada T; Zhang XY; Hayasaka Y Jpn J Ophthalmol; 2001; 45(4):355-8. PubMed ID: 11485765 [TBL] [Abstract][Full Text] [Related]
8. Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Fishman GA; Stone E; Gilbert LD; Vandenburgh K; Sheffield VC; Heckenlively JR Ophthalmology; 1994 Aug; 101(8):1409-21. PubMed ID: 8058286 [TBL] [Abstract][Full Text] [Related]
9. [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. PubMed ID: 12579739 [TBL] [Abstract][Full Text] [Related]
10. Polymorphic variations in peripherin-RDS gene in the Spanish population. Trujillo MJ; Ayuso C; Robledo M; Sandoval BG; Ramos C; Benitez J Ann Genet; 1995; 38(4):225-7. PubMed ID: 8629810 [TBL] [Abstract][Full Text] [Related]
11. Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS gene. Weleber RG; Carr RE; Murphey WH; Sheffield VC; Stone EM Arch Ophthalmol; 1993 Nov; 111(11):1531-42. PubMed ID: 8240110 [TBL] [Abstract][Full Text] [Related]
12. A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy. Bareil C; Hamel C; Arnaud B; Demaille J; Claustres M Ophthalmic Genet; 1997 Sep; 18(3):129-38. PubMed ID: 9361310 [TBL] [Abstract][Full Text] [Related]
13. Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance. Runte M; Dekomien G; Epplen JT Anim Genet; 2000 Jun; 31(3):223-7. PubMed ID: 10895316 [TBL] [Abstract][Full Text] [Related]
14. A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Gorin MB; Jackson KE; Ferrell RE; Sheffield VC; Jacobson SG; Gass JD; Mitchell E; Stone EM Ophthalmology; 1995 Feb; 102(2):246-55. PubMed ID: 7862413 [TBL] [Abstract][Full Text] [Related]
15. A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa. Sakuma H; Inana G; Murakami A; Yajima T; Weleber RG; Murphey WH; Gass JD; Hotta Y; Hayakawa M; Fujiki K Genomics; 1995 May; 27(2):384-6. PubMed ID: 7558016 [No Abstract] [Full Text] [Related]
16. A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa. Saga M; Mashima Y; Akeo K; Oguchi Y; Kudoh J; Shimizu N Hum Genet; 1993 Nov; 92(5):519-21. PubMed ID: 8244346 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of the peripherin/RDS gene as a candidate gene in families with age-related macular degeneration. Shastry BS; Trese MT Ophthalmologica; 1999; 213(3):165-70. PubMed ID: 10202289 [TBL] [Abstract][Full Text] [Related]
18. [Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes]. Benítez Del Castillo JM ; Trujillo MJ; Del Río T ; García B; Ayuso C; García Sánchez J Arch Soc Esp Oftalmol; 2000 Apr; 75(4):281-6. PubMed ID: 11151159 [TBL] [Abstract][Full Text] [Related]
19. [Genetic analysis of rhodopsin and peripherin genes in patients with autosomal dominant retinitis pigmentosa (adRP) in Polish families]. Brzeziańska E; Zdzieszyńska M; Goś R; Lewiński A Klin Oczna; 2004; 106(6):743-8. PubMed ID: 15787173 [TBL] [Abstract][Full Text] [Related]
20. Molecular screening of rhodopsin and peripherin/RDS genes in Mexican families with autosomal dominant retinitis pigmentosa. Matias-Florentino M; Ayala-Ramirez R; Graue-Wiechers F; Zenteno JC Curr Eye Res; 2009 Dec; 34(12):1050-6. PubMed ID: 19958124 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]