Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis

por Lu, Ya-Jie, Yao, Jun, Wei, Qin-Jun, Xing, Guang-Qian, Cao, Xin
Publicado 2015

IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family

por Li-Yang, Mei-Na, Shen, Xiao-Fei, Wei, Qin-Jun, Yao, Jun, Lu, Ya-Jie, Cao, Xin, Xing, Guang-Qian
Publicado 2015