Zhengqin Yin
5PUBLICATIONS
13CO-AUTHORS
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Publications (5)
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|May 10, 2021
Molecular genetics with clinical characteristics of Leber congenital amaurosis in the Han population of western China.Luyao Zhu, Wangbin Ouyang, Minfang Zhang
|May 07, 2020
Exosomes derived from neural progenitor cells preserve photoreceptors during retinal degeneration by inactivating microglia.Baishijiao Bian, Congjian Zhao, Xiangyu He
|Apr 23, 2020
Electrophysiological and Structural Changes in Chinese Patients with LHON.Min Wang, Hong Guo, Shiying Li
|Sep 25, 2019
SCF/SCFR signaling plays an important role in the early morphogenesis and neurogenesis of human embryonic neural retina.Yu Gong, Xiangyu He, Qiyou Li
|Aug 30, 2017
PRPF3-Associated Autosomal Dominant Retinitis Pigmentosa and CYP4V2-Associated Bietti's Crystalline Corneoretinal Dystrophy Coexist in a Multigenerational Chinese Family.Xiaohong Meng, Qiyou Li, Hong Guo
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