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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
3
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pubmed:dateCreated |
2003-6-6
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pubmed:abstractText |
To determine the mutation spectrum of the connexin 26 gene among 324 Taiwanese patients with prelingual deafness and the carrier rate of gene mutation in another 432 unrelated control subjects.
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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:issn |
1098-3600
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
161-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12792423-Alleles,
pubmed-meshheading:12792423-Child,
pubmed-meshheading:12792423-Child, Preschool,
pubmed-meshheading:12792423-Connexins,
pubmed-meshheading:12792423-DNA Mutational Analysis,
pubmed-meshheading:12792423-Deafness,
pubmed-meshheading:12792423-Heterozygote,
pubmed-meshheading:12792423-Humans,
pubmed-meshheading:12792423-Mutation,
pubmed-meshheading:12792423-Polymorphism, Genetic,
pubmed-meshheading:12792423-Taiwan
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pubmed:articleTitle |
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness.
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pubmed:affiliation |
Department of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei, Taiwan.
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pubmed:publicationType |
Journal Article,
Comparative Study
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