메뉴 건너뛰기




Volumn 14, Issue 3, 1999, Pages 263-266

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method

Author keywords

35delG mutation; Carrier frequency; GJB2 gene; Nonsyndromic recessive deafness; PCR mediated site directed mutagenesis

Indexed keywords

CONNEXIN 26;

EID: 0032840844     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)14:3<263::AID-HUMU10>3.0.CO;2-X     Document Type: Article
Times cited : (86)

References (13)
  • 1
    • 0030696315 scopus 로고    scopus 로고
    • Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: Implications for genetic studies in isolated populations
    • Carrasquillo MM, Zlotogora J, Barges S, Chakravarti A. 1997. Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. Hum Mol Genet 6:2163-2172.
    • (1997) Hum Mol Genet , vol.6 , pp. 2163-2172
    • Carrasquillo, M.M.1    Zlotogora, J.2    Barges, S.3    Chakravarti, A.4
  • 7
    • 0345055300 scopus 로고    scopus 로고
    • Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
    • Lench N, Houseman M, Newton V, Van Camp G, Mueller R. 1998a. Connexin-26 mutations in sporadic non-syndromal sensorineural deafness. Lancet 351:415-415.
    • (1998) Lancet , vol.351 , pp. 415-415
    • Lench, N.1    Houseman, M.2    Newton, V.3    Van Camp, G.4    Mueller, R.5
  • 10
    • 0026410464 scopus 로고
    • Genetic epidemiology of hearing impairment
    • Morton NE. 1991. Genetic epidemiology of hearing impairment. Ann NY Acad Sci 630:16-31.
    • (1991) Ann NY Acad Sci , vol.630 , pp. 16-31
    • Morton, N.E.1
  • 11
    • 0016468061 scopus 로고
    • Symposium on sensorineural hearing loss in children: Early detection and intervention. Genetic factors in deafness of early life
    • Nance WE, Sweeney A. 1975. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life. Otolaryngol Clin North Am 8:19-48.
    • (1975) Otolaryngol Clin North Am , vol.8 , pp. 19-48
    • Nance, W.E.1    Sweeney, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.