Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2009-8-26
pubmed:abstractText
The GJB2 gene, mapping to chromosome 13q12, encodes a gap junction protein, connexin 26, and is responsible for certain forms of congenital deafness, such as DFNB1 and DFNA3. Mutations of this gene are responsible for about one half of severe autosomal recessive non-syndromic deafness.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1423-0275
pubmed:author
pubmed:copyrightInfo
2009 S. Karger AG, Basel
pubmed:issnType
Electronic
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
212-5
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
High prevalence of the connexin 26 (GJB2) mutation in Chinese cochlear implant recipients.
pubmed:affiliation
Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't