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Journal Abstract Search

193 related items for PubMed ID: 9399908

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  • 4. Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.
    Corden LD, Swensson O, Swensson B, Smith FJ, Rochels R, Uitto J, McLEAN WH.
    Exp Eye Res; 2000 Jan; 70(1):41-9. PubMed ID: 10644419
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  • 5. Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.
    Chen YT, Tseng SH, Chao SC.
    Cornea; 2005 Nov; 24(8):928-32. PubMed ID: 16227835
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  • 8. A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.
    Yoon MK, Warren JF, Holsclaw DS, Gritz DC, Margolis TP.
    Br J Ophthalmol; 2004 Jun; 88(6):752-6. PubMed ID: 15148206
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  • 11. Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.
    Nichini O, Manzi Vd, Munier FL, Schorderet DF.
    Ophthalmic Genet; 2005 Dec; 26(4):169-73. PubMed ID: 16352477
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  • 18. Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations.
    Okada M, Yamamoto S, Inoue Y, Watanabe H, Maeda N, Shimomura Y, Ishii Y, Tano Y.
    Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1947-53. PubMed ID: 9727418
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  • 19. A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.
    Stewart H, Black GC, Donnai D, Bonshek RE, McCarthy J, Morgan S, Dixon MJ, Ridgway AA.
    Ophthalmology; 1999 May; 106(5):964-70. PubMed ID: 10328397
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