Xingle Zhao
4PUBLICATIONS
7CO-AUTHORS
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Publications (4)
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|Oct 08, 2025
Atypical phenotypic characteristics, mutation analysis and treatment in a family of riboflavin transporter deficiency caused by SLC52A3 variants.Peipei Li, Ting Zhang, Hongen Xu
|Aug 21, 2025
Gene therapy restores auditory function and rescues damaged inner hair cells in an aged Vglut3 knockout mouse model.Xingle Zhao, Hongen Xu, Chengyu Lian
|May 29, 2023
Cochlear transcript diversity and its role in auditory functions implied by an otoferlin short isoform.Huihui Liu, Hongchao Liu, Longhao Wang
|Jun 21, 2022
Gene Therapy Restores Auditory Functions in an Adult Vglut3 Knockout Mouse Model.Xingle Zhao, Huihui Liu, Hongchao Liu
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