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A Gja8 (Cx50) point mutation causes an alteration of α3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice

Academic Article
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  • Identity
  • Additional Document Info
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Overview

authors

  • Chang, B.
  • Wang, X.
  • Hawes, N. L.
  • Ojakian, R.
  • Davisson, M. T.
  • Lo, W. K.
  • Gong, Xiaohua

publication date

  • March 2002

journal

  • Human Molecular Genetics  Journal

subject areas

  • Amino Acid Substitution
  • Animals
  • Arginine
  • Base Sequence
  • Cataract
  • Chromosome Mapping
  • Codon
  • Connexins
  • Crosses, Genetic
  • Eye Proteins
  • Female
  • Genes, Dominant
  • Genetic Linkage
  • Genetic Markers
  • Genotype
  • Lens, Crystalline
  • Male
  • Mice
  • Mice, Inbred AKR
  • Mice, Inbred BALB C
  • Microphthalmos
  • Pedigree
  • Phenotype
  • Point Mutation
  • Sequence Analysis, DNA
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Identity

International Standard Serial Number (ISSN)

  • 0964-6906

Digital Object Identifier (DOI)

  • 10.1093/hmg/11.5.507

PubMed ID

  • 11875045
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Additional Document Info

start page

  • 507

end page

  • 513

volume

  • 11

issue

  • 5

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