reference/14234427

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14234427

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endingPage	2018
issn	1873-3468 0014-5793
issueIdentifier	15
pageRange	2008-2018
publicationName	FEBS Letters
startingPage	2008
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bibliographicCitation	Xia W, Hu J, Ma J, Huang J, Jing T, Deng L, Zhang J, Jiang N, Ma D, Ma Z. Mutations in TOP2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI3K‐Akt signalling pathway. FEBS Letters. 2019 Jun 26;593(15):2008–18. doi: 10.1002/1873-3468.13482.
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date	2019-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/31198993 https://doi.org/10.1002/1873-3468.13482
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations in TOP2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI3K‐Akt signalling pathway
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