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14. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa]. Cremers FP; Maugeri A; Klevering BJ; Hoefsloot LH; Hoyng CB Ned Tijdschr Geneeskd; 2002 Aug; 146(34):1581-4. PubMed ID: 12224481 [TBL] [Abstract][Full Text] [Related]
15. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Allikmets R Nat Genet; 1997 Sep; 17(1):122. PubMed ID: 9288113 [No Abstract] [Full Text] [Related]
16. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa. Klevering BJ; Maugeri A; Wagner A; Go SL; Vink C; Cremers FP; Hoyng CB Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334 [TBL] [Abstract][Full Text] [Related]
17. Stargardt's disease and the ABCR gene. Westerfeld C; Mukai S Semin Ophthalmol; 2008; 23(1):59-65. PubMed ID: 18214793 [TBL] [Abstract][Full Text] [Related]
18. Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family. Simonelli F; Testa F; Zernant J; Nesti A; Rossi S; Rinaldi E; Allikmets R Ophthalmic Res; 2004; 36(2):82-8. PubMed ID: 15017103 [TBL] [Abstract][Full Text] [Related]
19. Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. Sodi A; Bini A; Passerini I; Forconi S; Menchini U; Torricelli F Ophthalmic Surg Lasers Imaging; 2010; 41(1):48-53. PubMed ID: 20128570 [TBL] [Abstract][Full Text] [Related]
20. The ABCA4 gene and age-related macular degeneration: innocence or guilt by association. Gorin MB Arch Ophthalmol; 2001 May; 119(5):752-3. PubMed ID: 11346403 [No Abstract] [Full Text] [Related] [Next] [New Search]