| pubmed-article:21292415 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0009199 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C1709854 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0019904 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C1415077 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0163742 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:21292415 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
| pubmed-article:21292415 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:21292415 | pubmed:dateCreated | 2011-3-28 | lld:pubmed |
| pubmed-article:21292415 | pubmed:abstractText | This study aimed to investigate the prevalence of GJB2 gene for the 235delC mutations, the clinical features and the outcomes of patients who had undergone cochlear implantation. | lld:pubmed |
| pubmed-article:21292415 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21292415 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21292415 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21292415 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21292415 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21292415 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21292415 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:21292415 | pubmed:issn | 1879-1476 | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:NishiyamaNobu... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:SuzukiMamoruM | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:IkedaKatsuhis... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:KawanoAtsushi... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:YoshikawaSato... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:KawaguchiSach... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:FuruseHirokoH | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:HayashiChieri... | lld:pubmed |
| pubmed-article:21292415 | pubmed:author | pubmed-author:NakagawaMasah... | lld:pubmed |
| pubmed-article:21292415 | pubmed:copyrightInfo | Copyright © 2011 Elsevier Ireland Ltd. All rights reserved. | lld:pubmed |
| pubmed-article:21292415 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21292415 | pubmed:volume | 38 | lld:pubmed |
| pubmed-article:21292415 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21292415 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21292415 | pubmed:pagination | 444-9 | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:meshHeading | pubmed-meshheading:21292415... | lld:pubmed |
| pubmed-article:21292415 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21292415 | pubmed:articleTitle | The clinical features of patients with the homozygous 235delC and the compound-heterozygous Y136X/G45E of the GJB2 mutations (Connexin 26) in cochlear implant recipients. | lld:pubmed |
| pubmed-article:21292415 | pubmed:affiliation | The Open University of Japan, Japan. yoshikaway@aol.com | lld:pubmed |
| pubmed-article:21292415 | pubmed:publicationType | Journal Article | lld:pubmed |
