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.
159 related articles for article (PubMed ID: 11748859)
21. Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy. Itabashi T; Wada Y; Sato H; Kawamura M; Shiono T; Tamai M Am J Ophthalmol; 2004 Nov; 138(5):876-7. PubMed ID: 15531334 [TBL] [Abstract][Full Text] [Related]
22. Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier alleles. Zernant J; Külm M; Dharmaraj S; den Hollander AI; Perrault I; Preising MN; Lorenz B; Kaplan J; Cremers FP; Maumenee I; Koenekoop RK; Allikmets R Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3052-9. PubMed ID: 16123401 [TBL] [Abstract][Full Text] [Related]
24. Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis. Mellersh CS; Boursnell ME; Pettitt L; Ryder EJ; Holmes NG; Grafham D; Forman OP; Sampson J; Barnett KC; Blanton S; Binns MM; Vaudin M Genomics; 2006 Sep; 88(3):293-301. PubMed ID: 16806805 [TBL] [Abstract][Full Text] [Related]
25. CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis. Yzer S; Fishman GA; Racine J; Al-Zuhaibi S; Chakor H; Dorfman A; Szlyk J; Lachapelle P; van den Born LI; Allikmets R; Lopez I; Cremers FP; Koenekoop RK Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3736-44. PubMed ID: 16936081 [TBL] [Abstract][Full Text] [Related]
26. Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations. Al-Khayer K; Hagstrom S; Pauer G; Zegarra H; Sears J; Traboulsi EI Am J Ophthalmol; 2004 Feb; 137(2):375-7. PubMed ID: 14962443 [TBL] [Abstract][Full Text] [Related]
27. [From gene to disease; Leber congenital amaurosis (LCA)]. Yzer S; van den Born LI; Cremers FP; den Hollander AI Ned Tijdschr Geneeskd; 2005 Oct; 149(42):2334-7. PubMed ID: 16261712 [TBL] [Abstract][Full Text] [Related]
33. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Sohocki MM; Sullivan LS; Mintz-Hittner HA; Birch D; Heckenlively JR; Freund CL; McInnes RR; Daiger SP Am J Hum Genet; 1998 Nov; 63(5):1307-15. PubMed ID: 9792858 [TBL] [Abstract][Full Text] [Related]
34. Mechanisms of blindness: animal models provide insight into distinct CRX-associated retinopathies. Tran NM; Chen S Dev Dyn; 2014 Oct; 243(10):1153-66. PubMed ID: 24888636 [TBL] [Abstract][Full Text] [Related]
35. The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype. Hull S; Arno G; Plagnol V; Chamney S; Russell-Eggitt I; Thompson D; Ramsden SC; Black GC; Robson AG; Holder GE; Moore AT; Webster AR Invest Ophthalmol Vis Sci; 2014 Sep; 55(10):6934-44. PubMed ID: 25270190 [TBL] [Abstract][Full Text] [Related]
37. Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis. Simovich MJ; Miller B; Ezzeldin H; Kirkland BT; McLeod G; Fulmer C; Nathans J; Jacobson SG; Pittler SJ Hum Mutat; 2001 Aug; 18(2):164. PubMed ID: 11462243 [TBL] [Abstract][Full Text] [Related]
38. CrxRdy Cat: A Large Animal Model for CRX-Associated Leber Congenital Amaurosis. Occelli LM; Tran NM; Narfström K; Chen S; Petersen-Jones SM Invest Ophthalmol Vis Sci; 2016 Jul; 57(8):3780-92. PubMed ID: 27427859 [TBL] [Abstract][Full Text] [Related]
39. A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis. Ibrahim MT; Alarcon-Martinez T; Lopez I; Fajardo N; Chiang J; Koenekoop RK Sci Rep; 2018 Mar; 8(1):5034. PubMed ID: 29568065 [TBL] [Abstract][Full Text] [Related]
40. Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans. Kim DG; Joo K; Han J; Choi M; Kim SW; Park KH; Park SJ; Lee CS; Byeon SH; Woo SJ Genes (Basel); 2023 May; 14(5):. PubMed ID: 37239417 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]