Luping Zhang
6PUBLICATIONS
8CO-AUTHORS
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Publications (6)
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|May 14, 2025
Functional Correlation of Two Novel Nonsense POU4F3 Mutations Causing Late-Onset Progressive Nonsyndromic Hearing Loss in DFNA15 Families.Tianyang Zhang, Wei Wang, Luping Zhang
|Jul 03, 2024
A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family.Luping Zhang, Danya Zheng, Lian Xu
|May 23, 2022
A humanized murine model, demonstrating dominant progressive hearing loss caused by a novel KCNQ4 mutation (p.G228D) from a large Chinese family.Chong Cui, Luping Zhang, Fuping Qian
|Aug 11, 2020
THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis.Luping Zhang, Yu Gao, Ru Zhang
|Feb 13, 2020
Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.Di Wu, Weiyuan Huang, Zhenhang Xu
|Aug 21, 2018
Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss.Songqun Hu, Feifei Sun, Jie Zhang
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