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	Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway
	Xia, Wenjun; Hu, Jiongjiong; Ma, Jing; Huang, Jianbo; Jing, Tianrui; Deng, Lisha; Zhang, Jin; Jiang, Nan; Ma, Duan; Ma, Zhaoxin
刊名	FEBS LETTERS
	2019
卷号	593期号:15
关键词	deafness genes nonsyndromic hearing loss PI3K-Akt signalling pathway TOP2B zebrafish
ISSN号	1873-3468
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3597572
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Xia, Wenjun,Hu, Jiongjiong,Ma, Jing,et al. Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway[J]. FEBS LETTERS,2019,593(15).
APA	Xia, Wenjun.,Hu, Jiongjiong.,Ma, Jing.,Huang, Jianbo.,Jing, Tianrui.,...&Ma, Zhaoxin.(2019).Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway.FEBS LETTERS,593(15).
MLA	Xia, Wenjun,et al."Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway".FEBS LETTERS 593.15(2019).

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