Wenjun Xia

2PUBLICATIONS
1CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (2)

|Jun 25, 2019
Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.

Wenjun Xia, Jiongjiong Hu, Jing Ma

|Jul 06, 2017
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss.

Wenjun Xia, Jiongjiong Hu, Fei Liu

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