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J Med Genet. 2000 Jul;37(7):481-8.
Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.
PMID: 12011157 [PubMed - indexed for MEDLINE]
PMCID: PMC1735119
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Cited by 22 PubMed Central articles
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Analysis of single nucleotide polymorphisms of CRYGA and CRYGB genes in control population of western Indian origin.
Kapur S, Mehra S, Gajjar D, Vasavada A, Kapoor M, Sharad S, Alapure B, Rajkumar S.
Indian J Ophthalmol. 2009 May-Jun; 57(3):197-201.
[Indian J Ophthalmol. 2009]
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A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea.
Zhang L, Fu S, Ou Y, Zhao T, Su Y, Liu P.
Mol Vis. 2009; 15:276-82. Epub 2009 Feb 6.
[Mol Vis. 2009]
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A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family.
Yao K, Jin C, Zhu N, Wang W, Wu R, Jiang J, Shentu X.
Mol Vis. 2008 Jul 9; 14:1272-6. Epub 2008 Jul 9.
[Mol Vis. 2008]
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