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Journal Abstract Search

358 related items for PubMed ID: 32619608

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  • 3. Variants in the ABCA4 gene in a Brazilian population with Stargardt disease.
    Salles MV, Motta FL, Martin R, Filippelli-Silva R, Dias da Silva E, Varela P, Costa KA, Chiang JP, Pesquero JB, Sallum JF.
    Mol Vis; 2018; 24():546-559. PubMed ID: 30093795
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  • 7. Novel variants of ABCA4 in Han Chinese families with Stargardt disease.
    Hu FY, Gao FJ, Li JK, Xu P, Wang DD, Zhang SH, Wu JH.
    BMC Med Genet; 2020 Oct 31; 21(1):213. PubMed ID: 33129279
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  • 8. Screening of ABCA4 Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations.
    Jiang F, Pan Z, Xu K, Tian L, Xie Y, Zhang X, Chen J, Dong B, Li Y.
    Invest Ophthalmol Vis Sci; 2016 Jan 01; 57(1):145-52. PubMed ID: 26780318
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  • 9. Clinical and genetic characteristics of late-onset Stargardt's disease.
    Westeneng-van Haaften SC, Boon CJ, Cremers FP, Hoefsloot LH, den Hollander AI, Hoyng CB.
    Ophthalmology; 2012 Jun 01; 119(6):1199-210. PubMed ID: 22449572
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  • 13. Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease.
    Sangermano R, Bax NM, Bauwens M, van den Born LI, De Baere E, Garanto A, Collin RW, Goercharn-Ramlal AS, den Engelsman-van Dijk AH, Rohrschneider K, Hoyng CB, Cremers FP, Albert S.
    Ophthalmology; 2016 Jun 01; 123(6):1375-85. PubMed ID: 26976702
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  • 19. Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophy.
    Wawrocka A, Skorczyk-Werner A, Wicher K, Niedziela Z, Ploski R, Rydzanicz M, Sykulski M, Kociecki J, Weisschuh N, Kohl S, Biskup S, Wissinger B, Krawczynski MR.
    Mol Vis; 2018 Jun 01; 24():326-339. PubMed ID: 29769798
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  • 20. The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene.
    Klevering BJ, Deutman AF, Maugeri A, Cremers FP, Hoyng CB.
    Graefes Arch Clin Exp Ophthalmol; 2005 Feb 01; 243(2):90-100. PubMed ID: 15614537
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