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Journal Abstract Search

215 related items for PubMed ID: 22669729

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  • 23. [Autosomal dominant congenital golden crystal nuclear cataract caused by a missense mutation in gammaD crystallin gene (CRYGD) in a Chinese family].
    Gu JZ, Qi YH, Lin H, Li X, Wang J, Meng WM, Su H.
    Zhonghua Yan Ke Za Zhi; 2006 Oct; 42(10):913-7. PubMed ID: 17217786
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  • 26. Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
    Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):3937-44. PubMed ID: 17724170
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  • 28. Molecular genetic analysis of autosomal dominant late-onset cataract in a Chinese Family.
    Yang G, Zhong S, Zhang X, Peng B, Li J, Ke T, Xu H.
    J Huazhong Univ Sci Technolog Med Sci; 2010 Dec; 30(6):792-7. PubMed ID: 21181374
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  • 29. Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).
    VanderVeen DK, Andrews C, Nihalani BR, Engle EC.
    Mol Vis; 2011 Dec; 17():3333-8. PubMed ID: 22219628
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  • 30. Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
    Reis LM, Tyler RC, Muheisen S, Raggio V, Salviati L, Han DP, Costakos D, Yonath H, Hall S, Power P, Semina EV.
    Hum Genet; 2013 Jul; 132(7):761-70. PubMed ID: 23508780
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  • 31. Epidemiology and molecular genetics of congenital cataracts.
    Yi J, Yun J, Li ZK, Xu CT, Pan BR.
    Int J Ophthalmol; 2011 Jul; 4(4):422-32. PubMed ID: 22553694
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  • 32. Mutational screening of six genes in Chinese patients with congenital cataract and microcornea.
    Sun W, Xiao X, Li S, Guo X, Zhang Q.
    Mol Vis; 2011 Jul; 17():1508-13. PubMed ID: 21686328
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  • 35. Congenital coralliform cataract is the predominant consequence of a recurrent mutation in the CRYGD gene.
    Wang KJ, Wang JX, Wang JD, Li M, Zhang JS, Mao YY, Wan XH.
    Orphanet J Rare Dis; 2023 Jul 21; 18(1):200. PubMed ID: 37480084
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  • 36. Mutation screening of crystallin genes in Chinese families with congenital cataracts.
    Zhuang J, Cao Z, Zhu Y, Liu L, Tong Y, Chen X, Wang Y, Lu C, Ma X, Yang J.
    Mol Vis; 2019 Jul 21; 25():427-437. PubMed ID: 31523120
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  • 38. Novel human CRYGD rare variant in a Brazilian family with congenital cataract.
    de Figueirêdo ES, Giordano GG, Tavares A, da Silva MJ, de Vasconcellos JP, Arieta CE, de Melo MB.
    Mol Vis; 2011 Jul 21; 17():2207-11. PubMed ID: 21866214
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  • 39. Novel mutations in CRYGD are associated with congenital cataracts in Chinese families.
    Yang G, Chen Z, Zhang W, Liu Z, Zhao J.
    Sci Rep; 2016 Jan 06; 6():18912. PubMed ID: 26732753
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