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Journal Abstract Search

343 related items for PubMed ID: 15013897

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  • 3. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
    Tian X, Fujiki K, Zhang Y, Murakami A, Li Q, Kanai A, Wang W, Hao Y, Ma Z.
    Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
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  • 5. Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.
    Zenteno JC, Ramirez-Miranda A, Santacruz-Valdes C, Suarez-Sanchez R.
    Mol Vis; 2006 Apr 10; 12():331-5. PubMed ID: 16636649
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  • 11. Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene.
    Ołdak M, Szaflik JP, Ścieżyńska A, Udziela M, Maksym RB, Rymgayłło-Jankowska B, Hofmann-Rummelt C, Menzel-Severing J, Płoski R, Żarnowski T, Kruse FE, Szaflik J.
    Cornea; 2014 Mar 10; 33(3):294-9. PubMed ID: 24473223
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  • 13. TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
    Chakravarthi SV, Kannabiran C, Sridhar MS, Vemuganti GK.
    Invest Ophthalmol Vis Sci; 2005 Jan 10; 46(1):121-5. PubMed ID: 15623763
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  • 15. Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.
    Aldave AJ, Lin DY, Principe AH, Yellore VS, Weissman BA.
    Am J Ophthalmol; 2004 Jun 10; 137(6):1124-7. PubMed ID: 15183802
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