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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
2008-8-18
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pubmed:abstractText |
Mutations in the SLC26A4 gene are second only to GJB2 mutations as a currently identifiable genetic cause of sensorineural hearing loss. In most areas of China, genetic testing for sensorineural hearing loss is unavailable because of limited knowledge of the mutation spectrum. Although SLC26A4 c.919-2A>G (IVS7-2A>G) is a common mutation among some Asian populations, the mutation prevalence among various ethnic groups within China has not been studied.
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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 |
1530-0366
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pubmed:author |
pubmed-author:AhoAA,
pubmed-author:CHUE PEP,
pubmed-author:HanBingB,
pubmed-author:HanDongyiD,
pubmed-author:HuangDeliangD,
pubmed-author:KangDongyangD,
pubmed-author:MillerDavid TDT,
pubmed-author:PlattOrah SOS,
pubmed-author:ShaoHongH,
pubmed-author:SzeS HSH,
pubmed-author:TeL BLB,
pubmed-author:WuBai-LinBL,
pubmed-author:YuFeiF,
pubmed-author:YuanHuijunH,
pubmed-author:YuanYongyiY,
pubmed-author:ZhuQingwenQ
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pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
586-92
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pubmed:meshHeading |
pubmed-meshheading:18641518-Adolescent,
pubmed-meshheading:18641518-Asian Continental Ancestry Group,
pubmed-meshheading:18641518-Child,
pubmed-meshheading:18641518-Child, Preschool,
pubmed-meshheading:18641518-China,
pubmed-meshheading:18641518-Female,
pubmed-meshheading:18641518-Gene Frequency,
pubmed-meshheading:18641518-Genetic Variation,
pubmed-meshheading:18641518-Geography,
pubmed-meshheading:18641518-Hearing Loss, Sensorineural,
pubmed-meshheading:18641518-Humans,
pubmed-meshheading:18641518-Male,
pubmed-meshheading:18641518-Membrane Transport Proteins,
pubmed-meshheading:18641518-Mutation,
pubmed-meshheading:18641518-Prevalence,
pubmed-meshheading:18641518-Young Adult
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pubmed:year |
2008
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pubmed:articleTitle |
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.
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pubmed:affiliation |
Department of Otolaryngology and Genetic Testing Center for Deafness, Chinese PLA General Hospital, Beijing, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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