A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese family

por Liu, Jing, Jia, Yanlei, Wang, Lejin, Bu, Juan
Publicado 2016

Comparing myopic error in patients with basic and convergence insufficiency intermittent exotropia in China

por Meng, Qingyu, Wang, Lejin, Zhao, Mingwei, Wu, Xi, Guo, Lili
Publicado 2023

A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family

por Bu, Juan, He, Sijie, Wang, Lejin, Li, Jiankang, Liu, Jing, Zhang, Xiuqing
Publicado 2016

A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family

por Du, Wei, Bu, Juan, Dong, Jiamei, Jia, Yanlei, Li, Jing, Liang, Chen, Si, Shancheng, Wang, Lejin
Publicado 2011

Modified Posterior Scleral Reinforcement as a Treatment for High Myopia in Children and Its Therapeutic Effect

por Miao, Zequn, Li, Luojia, Meng, Xiaoli, Guo, Lili, Cao, Di, Jia, Yanlei, He, Dongmei, Huang, Lvzhen, Wang, Lejin
Publicado 2019

A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family

por Dong, Jiamei, Bu, Juan, Du, Wei, Li, Yuan, Jia, Yanlei, Li, Jianchang, Meng, Xiaoli, Yuan, Minghui, Peng, Xiaojuan, Zhou, Aimin, Wang, Lejin
Publicado 2012

Ultrathin and Robust Micro–Nano Composite Coating for Implantable Pressure Sensor Encapsulation

por Yao, Jialin, Qiang, Wenjiang, Wei, Hao, Xu, Yan, Wang, Bo, Zheng, Yushuang, Wang, Xizi, Miao, Zequn, Wang, Lejin, Wang, Song, Yang, Xing
Publicado 2020

FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome

por Jiang, Lei, Li, Yulei, Yang, Kangjuan, Wang, Yuping, Wang, Jiuxiang, Cui, Xiaoniu, Mao, Jinglin, Gao, Yong, Yi, Ping, Wang, Lejin, Liu, Jing Yu
Publicado 2020

Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family

por Zhang, Shirong, Liu, Mugen, Dong, Jia Mei, Yin, Ke, Wang, Pengyun, Bu, Juan, Li, Jing, Hao, Yan Sheng, Hao, Ping, Wang, Qing Kenneth, Wang, Lejin
Publicado 2008

p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus

por Li, Yulei, Jiang, Lei, Wang, Lejin, Wang, Cheng, Liu, Chunjie, Guo, Anyuan, Liu, Mugen, Zhang, Luoying, Ma, Cong, Zhang, Xianqin, Gao, Shangbang, Liu, Jing Yu
Publicado 2020

The critical role of m(6)A methylation in the pathogenesis of Graves' ophthalmopathy

por Zhu, Li, Li, Siyan, He, Shikun, Tong, Qizhe, Wang, Lejin, Li, Xiaohua, Wu, Xi, Meng, Qingyu, Jin, Enzhong, Zhang, Chuan, Li, Tianyuan, Xu, Ningda, Huang, Lvzhen, Wang, Yi, Zhao, Mingwei
Publicado 2020