Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study.
about
Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases.Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss.Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.
P2860
Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter study.
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Identification of a SNP in a r ...... g loss in a multicenter study.
@en
Identification of a SNP in a r ...... g loss in a multicenter study.
@nl
type
label
Identification of a SNP in a r ...... g loss in a multicenter study.
@en
Identification of a SNP in a r ...... g loss in a multicenter study.
@nl
prefLabel
Identification of a SNP in a r ...... g loss in a multicenter study.
@en
Identification of a SNP in a r ...... g loss in a multicenter study.
@nl
P2093
P50
P1476
Identification of a SNP in a r ...... g loss in a multicenter study.
@en
P2093
Daniëlle de Jong
Gertrude Hamader
Klemens Frei
Martin Ludwig
Reinhard Ramsebner
Wolf-Dieter Baumgartner
P304
P356
10.1097/MAO.0B013E31828D6501
P577
2013-06-01T00:00:00Z