Pu Dai
8PUBLICATIONS
7CO-AUTHORS
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Publications (8)
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|Mar 28, 2026
Therapeutic potential of cAMP-mediated lysosomal pH modulation in ATP6V1B2-related neuropathology.Lu Zheng, Weihao Zhao, Guang Yang
|Apr 05, 2023
Preimplantation genetic testing for hereditary hearing loss in Chinese population.Qingling Bi, Shasha Huang, Hui Wang
|Aug 18, 2020
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.Chang Guo, Sha-Sha Huang, Yong-Yi Yuan
|Feb 25, 2020
Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family.Shasha Huang, Xue Gao, Yufeng Wang
|Jun 01, 2018
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.Xue Gao, Jin-Cao Xu, Wei-Qian Wang
|Jul 12, 2017
Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.Xue Gao, Sha-Sha Huang, Yong-Yi Yuan
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