High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

Item
http://www.wikidata.org/entity/Q40248712
Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of ChinaA systematic review and meta-analysis of 235delC mutation of GJB2 geneGenetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients.The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency.Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate cases.
P2860

High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

Item
http://www.wikidata.org/entity/Q40248712
description
2006 nî lūn-bûn
@nan
2006年の論文
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2006年論文
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2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
High frequency of 35delG GJB2 ...... ith nonsyndromic hearing loss.
@en
type
label
High frequency of 35delG GJB2 ...... ith nonsyndromic hearing loss.
@en
prefLabel
High frequency of 35delG GJB2 ...... ith nonsyndromic hearing loss.
@en
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P356
P1433
P1476
High frequency of 35delG GJB2 ...... ith nonsyndromic hearing loss.
@en
P2093
P304
P31
P356
P433
P478
P577
P5875
P698