Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss
Wei, Qinjun, Zhu, Hongmei, Qian, Xuli, Chen, Zhibin, Yao, Jun, Lu, Yajie, Cao, Xin, Xing, Guangqian
Published in Journal of translational medicine (12.11.2014)
Published in Journal of translational medicine (12.11.2014)
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GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss
Xing, Guangqian, Yao, Jun, Liu, Chunyu, Wei, Qinjun, Qian, Xuli, Wu, Lingxin, Lu, Yajie, Cao, Xin
Published in Journal of medical genetics (01.06.2017)
Published in Journal of medical genetics (01.06.2017)
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Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations
Yao, Jun, Qian, Xuli, Bao, Jingxiao, Wei, Qinjun, Lu, Yajie, Zheng, Heng, Cao, Xin, Xing, Guangqian
Published in Scientific reports (02.06.2015)
Published in Scientific reports (02.06.2015)
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