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Journal Abstract Search

156 related items for PubMed ID: 21067486

  • 1. Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene.
    Liskova P, Filipec M, Merjava S, Jirsova K, Tuft SJ.
    Ophthalmic Genet; 2010 Dec; 31(4):230-4. PubMed ID: 21067486
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  • 2. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
    Lechner J, Dash DP, Muszynska D, Hosseini M, Segev F, George S, Frazer DG, Moore JE, Kaye SB, Young T, Simpson DA, Churchill AJ, Héon E, Willoughby CE.
    Invest Ophthalmol Vis Sci; 2013 May 03; 54(5):3215-23. PubMed ID: 23599324
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  • 3. Further genetic and clinical insights of posterior polymorphous corneal dystrophy 3.
    Liskova P, Palos M, Hardcastle AJ, Vincent AL.
    JAMA Ophthalmol; 2013 Oct 03; 131(10):1296-303. PubMed ID: 23807282
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  • 4. Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation.
    Nguyen DQ, Hosseini M, Billingsley G, Héon E, Churchill AJ.
    Acta Ophthalmol; 2010 Sep 03; 88(6):695-9. PubMed ID: 19432861
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  • 9. Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population.
    Vincent AL, Niederer RL, Richards A, Karolyi B, Patel DV, McGhee CN.
    Mol Vis; 2009 Dec 03; 15():2544-53. PubMed ID: 19997581
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  • 12. Posterior polymorphous corneal dystrophy 3 is associated with agenesis and hypoplasia of the corpus callosum.
    Jang MS, Roldan AN, Frausto RF, Aldave AJ.
    Vision Res; 2014 Jul 03; 100():88-92. PubMed ID: 24780443
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  • 14. Zeb1 mutant mice as a model of posterior corneal dystrophy.
    Liu Y, Peng X, Tan J, Darling DS, Kaplan HJ, Dean DC.
    Invest Ophthalmol Vis Sci; 2008 May 03; 49(5):1843-9. PubMed ID: 18436818
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  • 16. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
    Krafchak CM, Pawar H, Moroi SE, Sugar A, Lichter PR, Mackey DA, Mian S, Nairus T, Elner V, Schteingart MT, Downs CA, Kijek TG, Johnson JM, Trager EH, Rozsa FW, Mandal MN, Epstein MP, Vollrath D, Ayyagari R, Boehnke M, Richards JE.
    Am J Hum Genet; 2005 Nov 03; 77(5):694-708. PubMed ID: 16252232
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  • 17. Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
    Aldave AJ, Yellore VS, Yu F, Bourla N, Sonmez B, Salem AK, Rayner SA, Sampat KM, Krafchak CM, Richards JE.
    Am J Med Genet A; 2007 Nov 01; 143A(21):2549-56. PubMed ID: 17935237
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  • 19. Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus.
    Lam HY, Wiggs JL, Jurkunas UV.
    Cornea; 2010 Oct 01; 29(10):1180-5. PubMed ID: 20567203
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