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Volumn 64, Issue 6, 2003, Pages 517-518

Elevated frequencies of the 35delG allele of the connexin 26 gene in Corsica, France [1]

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; GENOMIC DNA; GUANINE;

EID: 0344740650     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1399-0004.2003.00175.x     Document Type: Letter
Times cited : (10)

References (12)
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    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 758-764
    • Van Camp, G.1    Willems, P.J.2    Smith, R.J.H.3
  • 2
    • 0344325111 scopus 로고    scopus 로고
    • R001 (available from
    • Van Camp G, Smith RJH. R001 (available from: http://www.uia.ac.be/dnalab/hhh).
    • Van Camp, G.1    Smith, R.J.H.2
  • 3
    • 12644276408 scopus 로고    scopus 로고
    • Linkage of DFNB1 to non-syndromic neurosensory autosomal recessive deafness in Mediterranean families
    • Gasparini P, Estivill X, Volpini V et al. Linkage of DFNB1 to non-syndromic neurosensory autosomal recessive deafness in Mediterranean families. Eur J Hum Genet 1997: 5: 83-88.
    • (1997) Eur. J. Hum. Genet. , vol.5 , pp. 83-88
    • Gasparini, P.1    Estivill, X.2    Volpini, V.3
  • 4
    • 0031007349 scopus 로고    scopus 로고
    • Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
    • Kelsell DP, Dunlop J, Stevens HP et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997: 387: 80-83.
    • (1997) Nature , vol.387 , pp. 80-83
    • Kelsell, D.P.1    Dunlop, J.2    Stevens, H.P.3
  • 5
    • 9844245885 scopus 로고    scopus 로고
    • Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal deafness (DFNB1) in Mediterraneans
    • Zelante L, Gasparini P, Estivill X et al. Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal deafness (DFNB1) in Mediterraneans. Hum Mol Genet 1997: 6: 1605-1609.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1605-1609
    • Zelante, L.1    Gasparini, P.2    Estivill, X.3
  • 6
    • 17544402026 scopus 로고    scopus 로고
    • High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG
    • Gasparini P, Rabionet R, Barbujani G et al. High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG. Eur J Hum Genet 2000: 8: 19-23.
    • (2000) Eur. J. Hum. Genet. , vol.8 , pp. 19-23
    • Gasparini, P.1    Rabionet, R.2    Barbujani, G.3
  • 7
    • 0034876240 scopus 로고    scopus 로고
    • Meta-analysis of GJB2 mutation 35delG frequencies in Europe
    • Lucotte G, Mercier G. Meta-analysis of GJB2 mutation 35delG frequencies in Europe. Genet Test 2001: 5: 149-152.
    • (2001) Genet. Test. , vol.5 , pp. 149-152
    • Lucotte, G.1    Mercier, G.2
  • 8
    • 0034881345 scopus 로고    scopus 로고
    • A common founder for the 35delG GJB gene mutation in connexin 26 hearing impairment
    • Van Laer L, Coucke P, Mueller RF et al. A common founder for the 35delG GJB gene mutation in connexin 26 hearing impairment. J Med Genet 2001: 38: 515-518.
    • (2001) J. Med. Genet. , vol.38 , pp. 515-518
    • Van Laer, L.1    Coucke, P.2    Mueller, R.F.3
  • 9
    • 0035129646 scopus 로고    scopus 로고
    • PCR test for diagnosis of the common GJB2-35delG mutation on dried blood spots and determination of the carrier frequency in France
    • Lucotte G, Bathelier C, Champenois T. PCR test for diagnosis of the common GJB2-35delG mutation on dried blood spots and determination of the carrier frequency in France. Mol Cell Probes 2001: 15: 57-59.
    • (2001) Mol. Cell Probes , vol.15 , pp. 57-59
    • Lucotte, G.1    Bathelier, C.2    Champenois, T.3
  • 10
    • 0036023041 scopus 로고    scopus 로고
    • Haplotypes of the Y chromosome in Corsica
    • [in French]
    • Lucotte G, Pinna A, Mercier G. Haplotypes of the Y chromosome in Corsica. CR Biol 2002: 325: 191-196 [in French].
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  • 11
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    • Connexin-26 mutations in sporadic and inherited sensorineural deafness
    • Estivill X, Fortina P, Surrey S et al. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet 1998: 351: 394-398.
    • (1998) Lancet , vol.351 , pp. 394-398
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  • 12
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    • High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness
    • Antoniadi T, Rabionet R, Kroupis C et al. High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness. Clin Genet 1999: 55: 581-582.
    • (1999) Clin. Genet. , vol.55 , pp. 581-582
    • Antoniadi, T.1    Rabionet, R.2    Kroupis, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.