Yanqiu Liu
2PUBLICATIONS
1CO-AUTHORS

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Publications (2)
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|Apr 27, 2024
Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA.Yan Yang, Haiyan Luo, Lijuan Pan
|Jan 22, 2020
A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family.Jia Chen, Huizhen Yuan, Kang Xie
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