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      Genetic association of TCF4 intronic polymorphisms, CTG18.1 and rs17089887, with Fuchs' endothelial corneal dystrophy in an Indian population.

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          Abstract

          To assess the genetic association of transcription factor 4 (TCF4) intronic polymorphisms and CTG18.1 allele in individuals with Fuchs' endothelial corneal dystrophy (FECD) individuals from a sample Indian population.

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          Author and article information

          Journal
          Invest. Ophthalmol. Vis. Sci.
          Investigative ophthalmology & visual science
          1552-5783
          0146-0404
          Oct 23 2014
          : 55
          : 11
          Affiliations
          [1 ] School of Biological Sciences, National Institute of Science Education and Research, Bhubaneswar, India.
          [2 ] Cornea and Anterior Segment Services, L. V. Prasad Eye Institute, Bhubaneswar, India.
          Article
          iovs.14-15297
          10.1167/iovs.14-15297
          25342617
          Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.

          Fuchs' dystrophy, SNP, TCF4, genetic association

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