Randomized controlled trial on the efficacy and safety of autologous serum eye drops in dry eye syndrome

por Zheng, Na, Zhu, Si-Quan
Publicado 2023

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

por Wang, Kai Jie, Zhu, Si Quan
Publicado 2012

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-crystall...

por Wang, Kai Jie, Wang, Sha, Cao, Ni-Qian, Yan, Yong-Bin, Zhu, Si Quan
Publicado 2011

A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts

por Ma, Xu, Li, Fei-Feng, Wang, Shu-Zhen, Gao, Chang, Zhang, Meng, Zhu, Si-Quan
Publicado 2008

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

por Wang, Kai Jie, Li, Sha Sha, Yun, Bo, Ma, Wen Xian, Jiang, Tian Ge, Zhu, Si Quan
Publicado 2011

Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts

por Li, Fei-feng, Zhu, Si-quan, Wang, Shu-zhen, Gao, Chang, Huang, Shang-zhi, Zhang, Meng, Ma, Xu
Publicado 2008

The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia

por Zhao, Yan Yan, Zhang, Feng Ju, Zhu, Si Quan, Duan, Hui, Li, Yang, Zhou, Zhong Jun, Ma, Wen Xian, Li Wang, Ning
Publicado 2011