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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
9100
|
| pubmed:dateCreated |
1998-3-18
|
| pubmed:grant | |
| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0140-6736
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
7
|
| pubmed:volume |
351
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
415
|
| pubmed:dateRevised |
2009-9-29
|
| pubmed:meshHeading |
pubmed-meshheading:9482297-Child,
pubmed-meshheading:9482297-Cohort Studies,
pubmed-meshheading:9482297-Connexins,
pubmed-meshheading:9482297-DNA Mutational Analysis,
pubmed-meshheading:9482297-Deafness,
pubmed-meshheading:9482297-Humans,
pubmed-meshheading:9482297-Infant, Newborn,
pubmed-meshheading:9482297-Mutation
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness.
|
| pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
|