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Journal Abstract Search

203 related items for PubMed ID: 18334946

  • 1. A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
    Vanita V, Singh JR, Singh D, Varon R, Sperling K.
    Mol Vis; 2008 Feb 09; 14():323-6. PubMed ID: 18334946
    [Abstract] [Full Text] [Related]

  • 2. A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
    Vanita V, Singh JR, Singh D, Varon R, Sperling K.
    Mol Vis; 2008 Jun 17; 14():1171-5. PubMed ID: 18587493
    [Abstract] [Full Text] [Related]

  • 3. A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
    Vanita V, Hennies HC, Singh D, Nürnberg P, Sperling K, Singh JR.
    Mol Vis; 2006 Oct 18; 12():1217-22. PubMed ID: 17110920
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  • 5. A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree.
    Hu S, Wang B, Zhou Z, Zhou G, Wang J, Ma X, Qi Y.
    Mol Vis; 2010 Aug 11; 16():1585-92. PubMed ID: 20806042
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  • 7. A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract.
    Yan M, Xiong C, Ye SQ, Chen Y, Ke M, Zheng F, Zhou X.
    Mol Vis; 2008 Mar 04; 14():418-24. PubMed ID: 18334966
    [Abstract] [Full Text] [Related]

  • 8. A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family.
    Gao X, Cheng J, Lu C, Li X, Li F, Liu C, Zhang M, Zhu S, Ma X.
    Curr Eye Res; 2010 Jul 04; 35(7):597-604. PubMed ID: 20597646
    [Abstract] [Full Text] [Related]

  • 9. A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.
    Wang K, Wang B, Wang J, Zhou S, Yun B, Suo P, Cheng J, Ma X, Zhu S.
    Mol Vis; 2009 Dec 16; 15():2813-20. PubMed ID: 20019893
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  • 11. A novel p.F206I mutation in Cx46 associated with autosomal dominant congenital cataract.
    Wang KJ, Zhu SQ.
    Mol Vis; 2012 Dec 16; 18():968-73. PubMed ID: 22550389
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  • 16. Mutation analysis in Chinese families with autosomal dominant hereditary cataracts.
    Yang Z, Li Q, Ma X, Zhu SQ.
    Curr Eye Res; 2015 Dec 16; 40(12):1225-31. PubMed ID: 25549162
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  • 18. A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.
    Li J, Wang Q, Fu Q, Zhu Y, Zhai Y, Yu Y, Zhang K, Yao K.
    Mol Vis; 2013 Dec 16; 19():767-74. PubMed ID: 23592913
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  • 19. Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
    Vanita V, Singh JR, Singh D, Varon R, Sperling K.
    Mol Vis; 2009 Dec 16; 15():476-81. PubMed ID: 19262743
    [Abstract] [Full Text] [Related]

  • 20. Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
    Devi RR, Vijayalakshmi P.
    Mol Vis; 2006 Mar 23; 12():190-5. PubMed ID: 16604058
    [Abstract] [Full Text] [Related]

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