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19199245
Source:
http://linkedlifedata.com/resource/pubmed/id/19199245
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008565
,
umls-concept:C0030705
,
umls-concept:C0220908
,
umls-concept:C1384666
,
umls-concept:C1418445
,
umls-concept:C2677304
pubmed:issue
1
pubmed:dateCreated
2009-2-9
pubmed:abstractText
To study the SLC26A4 gene mutations in patients with nonsyndromic hearing loss (NSHL) and provide the clinical guidance of gene diagnosis.
pubmed:language
chi
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/SLC26A4 protein, human
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1003-9406
pubmed:author
pubmed-author:FengYongY
,
pubmed-author:LiHong-yanHY
,
pubmed-author:LiangDe-shengDS
,
pubmed-author:PanQianQ
,
pubmed-author:WuLing-qianLQ
,
pubmed-author:ZhaoJuanJ
,
pubmed-author:ZhaoKaiK
pubmed:issnType
Print
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
21-5
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:19199245-Adolescent
,
pubmed-meshheading:19199245-Adult
,
pubmed-meshheading:19199245-Base Sequence
,
pubmed-meshheading:19199245-Child
,
pubmed-meshheading:19199245-Child, Preschool
,
pubmed-meshheading:19199245-Chromatography, High Pressure Liquid
,
pubmed-meshheading:19199245-DNA Mutational Analysis
,
pubmed-meshheading:19199245-Genetic Testing
,
pubmed-meshheading:19199245-Genotype
,
pubmed-meshheading:19199245-Hearing Loss
,
pubmed-meshheading:19199245-Humans
,
pubmed-meshheading:19199245-Infant
,
pubmed-meshheading:19199245-Membrane Transport Proteins
,
pubmed-meshheading:19199245-Mutation
,
pubmed-meshheading:19199245-Phenotype
,
pubmed-meshheading:19199245-Polymorphism, Genetic
pubmed:year
2009
pubmed:articleTitle
[Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography].
pubmed:affiliation
National Laboratory of Medical Genetics, Central South University, Changsha, Hunan, 410078 P. R. China. wulingqian@sklmg.edu.cn.
pubmed:publicationType
Journal Article
,
English Abstract