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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 20, 2024. (Total: 231655Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Hearing Loss and DFNA5[original query]
A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing loss.
Annals of human genetics 2014 Mar 78 (2): 83-91.
Nishio Ayako, Noguchi Yoshihiro, Sato Tatsuya, Naruse Taeko K, Kimura Akinori, Takagi Akira, Kitamura K
Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study.
Environmental health : a global access science source 2015 14 (1): 77.
Zhang Xuhui, Liu Yi, Zhang Lei, Yang Zhangping, Yang Luoxian, Wang Xuchu, Jiang CaiXia, Wang Qiang, Xia Yuyong, Chen Yanjuan, Wu Ou, Zhu Yim
Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing.
Gene 2022 2 819 146258.
Liu Ya, Tan Meihua, Cai Luhang, Lv Lihui, Chen Qingqing, Chen Wei, Yang Hang, Xu Yapi
Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss.
Diagnostics (Basel, Switzerland) 2022 1 12 (1): .
Mansard Luke, Vaché Christel, Bianchi Julie, Baudoin Corinne, Perthus Isabelle, Isidor Bertrand, Blanchet Catherine, Baux David, Koenig Michel, Kalatzis Vasiliki, Roux Anne-Françoi
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