Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
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Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencingDiagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-AnalysisGJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing LossMolecular screening of patients with nonsyndromic hearing loss from Nanjing city of ChinaHereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication.A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean populationPrevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.Functional evaluation of GJB2 variants in nonsyndromic hearing loss.A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian familyMutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, ChinaScreening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in KoreansA systematic review and meta-analysis of 235delC mutation of GJB2 geneTargeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.Construction of a DNA chip for screening of genetic hearing loss.A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family.A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct.Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.Long Term Speech Perception Outcomes of Cochlear Implantation in Gap Junction Protein Beta 2 Related Hearing Loss.Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities.Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China.Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.
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P2860
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 27 June 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@en
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@nl
type
label
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@en
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@nl
prefLabel
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@en
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@nl
P2093
P2860
P1476
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
@en
P2093
P2860
P304
P356
10.1016/J.IJPORL.2008.05.007
P577
2008-06-27T00:00:00Z