Wang L - Search Results

1

[TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy].

Qi YH, He HD, Li Y, Wang L, Lin H, Su H, Gu JZ, Huang SZ. Qi YH, et al. Among authors: wang l. Zhonghua Yan Ke Za Zhi. 2007 Aug;43(8):718-21. Zhonghua Yan Ke Za Zhi. 2007. PMID: 18001570 Chinese.

2

A new congenital nuclear cataract caused by a missense mutation in the gammaD-crystallin gene (CRYGD) in a Chinese family.

Gu J, Qi Y, Wang L, Wang J, Shi L, Lin H, Li X, Su H, Huang S. Gu J, et al. Among authors: wang l, wang j. Mol Vis. 2005 Nov 9;11:971-6. Mol Vis. 2005. PMID: 16288201 Free article.

3

A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y. Wang L, et al. Mol Vis. 2007 Aug 1;13:1357-62. Mol Vis. 2007. PMID: 17768382

4

[A novel missense mutation in MIP gene resulted in polymorphic cataract].

Lin H, Wang L, Zhou N, Su H, Gu J, Qi Y. Lin H, et al. Among authors: wang l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):6-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247294 Chinese.

5

An atypical phenotype of Reis-Bücklers corneal dystrophy caused by the G623D mutation in TGFBI.

Li D, Qi Y, Wang L, Lin H, Zhou N, Zhao L. Li D, et al. Among authors: wang l. Mol Vis. 2008 Jul 11;14:1298-302. Mol Vis. 2008. PMID: 18636123 Free PMC article.

6

Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallin.

Wang L, Lin H, Gu J, Su H, Huang S, Qi Y. Wang L, et al. Ophthalmic Res. 2009;41(3):148-53. doi: 10.1159/000209668. Epub 2009 Mar 26. Ophthalmic Res. 2009. PMID: 19321936

7

Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6.

Dang X, Zhu Q, Wang L, Su H, Lin H, Zhou N, Liang T, Wang Z, Huang S, Ren Q, Qi Y. Dang X, et al. Among authors: wang l, wang z. Mol Vis. 2009;15:700-5. Epub 2009 Apr 6. Mol Vis. 2009. PMID: 19365571 Free PMC article.

8

A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family.

Wang L, Chen X, Lu Y, Wu J, Yang B, Sun X. Wang L, et al. Mol Vis. 2011 Mar 26;17:804-9. Mol Vis. 2011. PMID: 21527994 Free PMC article.

9

Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract.

Wang L, Luo Y, Wen W, Zhang S, Lu Y. Wang L, et al. Mol Vis. 2011;17:2380-5. Epub 2011 Sep 1. Mol Vis. 2011. PMID: 21921990 Free PMC article.

10

Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract.

Wang L, Chen Y, Chen X, Sun X. Wang L, et al. Indian J Ophthalmol. 2016 Jul;64(7):508-12. doi: 10.4103/0301-4738.190139. Indian J Ophthalmol. 2016. PMID: 27609163 Free PMC article.

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