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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2011-3-28
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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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1879-1476
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
444-9
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pubmed:meshHeading |
pubmed-meshheading:21292415-Adult,
pubmed-meshheading:21292415-Alleles,
pubmed-meshheading:21292415-Child, Preschool,
pubmed-meshheading:21292415-Cochlear Implants,
pubmed-meshheading:21292415-Connexins,
pubmed-meshheading:21292415-Female,
pubmed-meshheading:21292415-Gene Deletion,
pubmed-meshheading:21292415-Hearing,
pubmed-meshheading:21292415-Hearing Loss, Sensorineural,
pubmed-meshheading:21292415-Heterozygote,
pubmed-meshheading:21292415-Homozygote,
pubmed-meshheading:21292415-Humans,
pubmed-meshheading:21292415-Male,
pubmed-meshheading:21292415-Mutation,
pubmed-meshheading:21292415-Software,
pubmed-meshheading:21292415-Treatment Outcome
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pubmed:year |
2011
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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.
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pubmed:affiliation |
The Open University of Japan, Japan. yoshikaway@aol.com
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pubmed:publicationType |
Journal Article
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