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Volumn 35, Issue 2, 1998, Pages 151-152

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)

Author keywords

Connexin 26 (GJB2); DFNB1 DFNA3; Sensorineural hearing loss

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN; MUTANT PROTEIN; UNCLASSIFIED DRUG;

EID: 0031982160     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.2.151     Document Type: Article
Times cited : (30)

References (4)
  • 1
    • 0031007349 scopus 로고    scopus 로고
    • Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
    • Kelsell DP, Dunlop J, Stevens HP, et a!. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997;387:80-3.
    • (1997) Nature , vol.387 , pp. 80-83
    • Kelsell, D.P.1    Dunlop, J.2    Stevens, H.P.3
  • 2
    • 0030028301 scopus 로고
    • The gap junction communication channel
    • Kumar NM, Gilula NB. The gap junction communication channel. Cell 1994;84:381-8.
    • (1994) Cell , vol.84 , pp. 381-388
    • Kumar, N.M.1    Gilula, N.B.2
  • 3
    • 0030946546 scopus 로고    scopus 로고
    • Nonsyndromic hearing impairment: Unparalleled heterogeneity
    • Van Camp G, Willems PJ, Smith RJH. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 1997;60;758-65.
    • (1997) Am J Hum Genet , vol.60 , pp. 758-765
    • Van Camp, G.1    Willems, P.J.2    Smith, R.J.H.3
  • 4
    • 33749742705 scopus 로고
    • The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population
    • Maw MA, Allen-Powell DR, Goodey RJ, a al. The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population. Am J Hum Gcna 1995;S7:62935.
    • (1995) Am J Hum Gcna , vol.7 , pp. 62935
    • Maw, M.A.1    Allen-Powell, D.R.2    Goodey, R.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.