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[期刊论文] 作者：Wenjun Xia,Fei Liu,Duan Ma,
来源：医学前沿 年份：2016
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SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic midfrequency hearing
[会议论文] 作者：Zhaoxin Ma,Wenjun Xia,Fei Liu,Jing Ma,Shaoyang Sun,Jin Zhang,Nan Jiang,Xu Wang,Jiongjiong Hu,Duan Ma,
来源：中国生物化学与分子生物学会2016年全国学术会议 年份：2016
Hearing impairment is considered one of the most prevalent clinic disability worldwide.The variety of hearing impairment causative genes determines the diversity of pathogenic machanism.In our studies...
Down-regulation Of Msrb3 And Destruction Of Normal Auditory System Development Through Hair Cell Apo
[会议论文] 作者：Fei Liu,Nan Jiang,Yingzhi Wang,Shaoyang Sun,Huijun Wang,Xu Wang,Jing Ma,Xiaofang Shen,Jin Zhang,Wenjun Xia,
来源：第十四次全国医学遗传学学术会议 年份：2015
Hearing defects can significantly influence quality of life for those who experience them.At this time, 177 deafness genes have been cloned, including 134 n...
Down-regulation Of Msrb3 And Destruction Of Normal Auditory System Development Through Hair Cell Apo
[会议论文] 作者：Xiaofang Shen,Fei Liu,Yingzhi Wang,Huijun Wang,Jing Ma,Wenjun Xia,Jin Zhang,Nan Jiang,Shaoyang Sun,Xu,
来源：第十四次全国医学遗传学学术会议 年份：2015
Hearing defects can significantly influence quality of life for those who experience them.At this time, 177 deafness genes have been cloned, including 134 non-syndromic hearing-loss genes....
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