Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family

Ítems similars

• Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)
  per: Zhou, Zhou, et al.
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• A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree
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• A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  per: Yang, Guoxing, et al.
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• A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene
  per: Guleria, Kamlesh, et al.
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• A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract
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