Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family

Por Liu, Xiaowen, Tang, Zhaohui, Li, Chang, Yang, Kangjuan, Gan, Guanqi, Zhang, Zibo, Liu, Jingyu, Jiang, Fagang, Wang, Qing, Liu, Mugen
Publicado em 2010

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 no Invest Ophthalmol Vis Sci (2020)