Wenjun Xia

Years Active: 2017-2019
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Wenjun Xia, Jiongjiong Hu, Jing Ma, Jianbo Huang, Xu Wang, Nan Jiang, Jin Zhang, Zhaoxin Ma, Duan Ma
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss. Clinical genetics 96 (4) (2019)
Wenjun Xia, Jiongjiong Hu, Fei Liu, Jing Ma, Shaoyang Sun, Jin Zhang, Kaiyue Jin, Jianbo Huang, Nan Jiang, Xu Wang, Wen Li, Zhaoxin Ma, Duan Ma
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss. Human mutation 38 (10) (2017)

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