reference/26318852

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26318852

Outgoing Links

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contentType	Journal Article\|Randomized Controlled Trial\|Research Support, Non-U.S. Gov't
endingPage	617
issn	1434-5161 1435-232X
issueIdentifier	10
pageRange	613-617
publicationName	Journal of Human Genetics
startingPage	613
bibliographicCitation	Taniguchi M, Matsuo H, Shimizu S, Nakayama A, Suzuki K, Hamajima N, Shinomiya N, Nishio S, Kosugi S, Usami S, Ito J, Kitajiri S. Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population. Journal of Human Genetics. 2015 Jul 16;60(10):613–7. doi: 10.1038/jhg.2015.82.
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date	2015-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1038/jhg.2015.82 https://pubmed.ncbi.nlm.nih.gov/PMC4635169 https://pubmed.ncbi.nlm.nih.gov/26178431
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Carrier frequency of the GJB2 mutations that cause hereditary hearing loss in the Japanese population
discusses	http://id.nlm.nih.gov/mesh/M0490170 http://id.nlm.nih.gov/mesh/M0220781 http://id.nlm.nih.gov/mesh/M0026696
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Incoming Links

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Total number of triples: 43.