K. Wang

发表

Novel beta-crystallin gene mutations in Chinese families with nuclear cataracts.

Xu Ma, Fengju Zhang, Fengju Zhang, 2011, Archives of ophthalmology.

A novel p.F206I mutation in Cx46 associated with autosomal dominant congenital cataract

Si-quan Zhu, K. Wang, 2012, Molecular vision.

Novel -Crystallin Gene Mutations in Chinese Families With Nuclear Cataracts

Fengju Zhang, Si-quan Zhu, K. Wang, 2011 .

A Novel p.G112E Mutation in BFSP2 Associated with Autosomal Dominant Pulverulent Cataract with Sutural Opacities

Si-quan Zhu, K. Wang, Qing Liu, 2014, Current eye research.

Congenital coralliform cataract is the predominant consequence of a recurrent mutation in the CRYGD gene

X. Wan, K. Wang, Yingyan Mao, 2023, Orphanet Journal of Rare Diseases.

A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family

Sha Sha Li, Si-quan Zhu, W. Ma, 2011, Molecular vision.

Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract

Xu Zha, Si-quan Zhu, K. Wang, 2018, Current eye research.

Identification of the p. R116H mutation in a Chinese Family with Novel Variable Cataract Phenotype: Evidence for a Mutational Hot Spot in αA-Crystallin Gene

Binbin Wang, Jing Wang, Xu Ma, 2012, Ophthalmic genetics.

A Novel Mutation in CRYBB1 Associated with Congenital Cataract-Microcornea Syndrome: The p.Ser129Arg Mutation Destabilizes the βB1/βA3-crystallin Heteromer But Not the βB1-crystallin Homomer

Yong-Bin Yan, Si-quan Zhu, K. Wang, 2011, Human mutation.