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Zixi Sun

Showing results (41-50 of 45) with videos related to

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Investigative Ophthalmology & Visual Science|April 15, 2025
A Novel AAV Capsid-Mediated RS1 Gene Therapy Restored Retinal Function to Wild-Type Levels in Rs1R213W Mouse ModelXing Wei, Sisi Ma, Yunyu Zhou, et al.
Human Molecular Genetics|August 8, 2018
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosaLin Zhang, Zixi Sun, Peiquan Zhao, et al.
Science Advances|September 7, 2022
Mutations in <i>BCOR</i>, a co-repressor of <i>CRX/OTX2</i>, are associated with early-onset retinal degenerationMaéva Langouët, Christine Jolicoeur, Awais Javed, et al.
American Journal of Ophthalmology|July 25, 2020
Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2Lizhu Yang, Kwangsic Joo, Kazushige Tsunoda, et al.
American Journal of Human Genetics|March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental AnomaliesMingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Investigative Ophthalmology & Visual Science|April 15, 2025
A Novel AAV Capsid-Mediated RS1 Gene Therapy Restored Retinal Function to Wild-Type Levels in Rs1R213W Mouse ModelXing Wei, Sisi Ma, Yunyu Zhou, et al.
Human Molecular Genetics|August 8, 2018
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosaLin Zhang, Zixi Sun, Peiquan Zhao, et al.
Science Advances|September 7, 2022
Mutations in <i>BCOR</i>, a co-repressor of <i>CRX/OTX2</i>, are associated with early-onset retinal degenerationMaéva Langouët, Christine Jolicoeur, Awais Javed, et al.
American Journal of Ophthalmology|July 25, 2020
Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2Lizhu Yang, Kwangsic Joo, Kazushige Tsunoda, et al.
American Journal of Human Genetics|March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental AnomaliesMingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
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