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Author/Creator He, Chufeng

1. A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans. Issue 5 (1st September 2022)

Authors:
Huang, Sida; Ma, Lu; Liu, Xuezhong; He, Chufeng; Li, Jiada; Hu, Zhengmao; Jiang, Lu; Liu, Yalan; Liu, Xianlin; Feng, Yong; Cai, Xinzhang
Journal:
Human molecular genetics
Issue:
Volume 32:Issue 5(2023)
Page Start:
720
Record Type:
Journal Article
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2. Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family. (September 2017)

Authors:
Niu, Zhijie; Feng, Yong; Hu, Zhengmao; Li, Jiada; Sun, Jie; Chen, Hongsheng; He, Chufeng; Wang, Xueping; Jiang, Lu; Liu, Yalan; Cai, Xinzhang; Wang, Lili; Cai, Yuxiang; Liu, Xuezhong; Mei, Lingyun
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 100(2017:Sep.)
Page Start:
1
Record Type:
Journal Article
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5. Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families. (December 2018)

Authors:
Deng, Yuyuan; Sang, Shushan; Wen, Jie; Liu, Yalan; Ling, Jie; Chen, Hongsheng; Cai, Xinzhang; Mei, Lingyun; Chen, Xiaoya; Li, Meng; Li, Wu; Li, Taoxi; He, Chufeng; Feng, Yong
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 115(2018:Dec.)
Page Start:
114
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗