Literature DB >> 9482297

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness.

N Lench, M Houseman, V Newton, G Van Camp, R Mueller.   

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Year:  1998        PMID： 9482297     DOI： 10.1016/s0140-6736(98)24006-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  19 in total

1.  Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

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Review 2.  Connexin mutations in skin disease and hearing loss.

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3.  Cx26 deafness: mutation analysis and clinical variability.

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4.  Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.

Authors:  Yongyi Yuan; Fei Yu; Guojian Wang; Shasha Huang; Ruili Yu; Xin Zhang; Deliang Huang; Dongyi Han; Pu Dai
Journal:  J Transl Med       Date:  2010-12-02       Impact factor: 5.531

5.  GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.

Authors:  Elif Baysal; Yildirim A Bayazit; Serdar Ceylaner; Necat Alatas; Buket Donmez; Gulay Ceylaner; Imran San; Baki Korkmaz; Akin Yilmaz; Adnan Menevse; Senay Altunyay; Bulent Gunduz; Nebil Goksu; Ahmet Arslan; Abdullah Ekmekci
Journal:  J Genet       Date:  2008-04       Impact factor: 1.166

6.  GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment.

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7.  A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.

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Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

8.  Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran.

Authors:  Hamid Galehdari; Ali Mohammad Foroughmand; Maryam Naderi Soorki; Gholamreza Mohammadian
Journal:  Indian J Hum Genet       Date:  2009-01

9.  Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis.

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Journal:  J Transl Med       Date:  2008-11-30       Impact factor: 5.531

10.  Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.

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Journal:  J Transl Med       Date:  2009-09-10       Impact factor: 5.531
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