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Volumn 8, Issue 12, 2002, Pages 1332-1333

Selection for deafness? [1]

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; SODIUM; CONNEXIN 26; GAP JUNCTION PROTEIN;

EID: 0036887084     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/nm1202-1332     Document Type: Letter
Times cited : (61)

References (9)
  • 2
    • 0023663697 scopus 로고
    • What maintains the frequencies of human genetic diseases?
    • Rotter, J.I. & Diamond, J.M. What maintains the frequencies of human genetic diseases? Nature 329, 289-290 (1987).
    • (1987) Nature , vol.329 , pp. 289-290
    • Rotter, J.I.1    Diamond, J.M.2
  • 3
    • 0035968605 scopus 로고    scopus 로고
    • Advances in hereditary deafness
    • Tekin, M. Arnos, K.S. & Pandya, A. Advances in hereditary deafness. Lancet 358, 1082-1090 (2001).
    • (2001) Lancet , vol.358 , pp. 1082-1090
    • Tekin, M.1    Arnos, K.S.2    Pandya, A.3
  • 4
    • 17544402026 scopus 로고    scopus 로고
    • High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG
    • Gasparini, P. et al. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG. Eur. J. Hum. Genet. 8, 19-23 (2000).
    • (2000) Eur. J. Hum. Genet. , vol.8 , pp. 19-23
    • Gasparini, P.1
  • 6
    • 0035226626 scopus 로고    scopus 로고
    • Connexin disorders of the skin
    • Richard, G. Connexin disorders of the skin. Adv. Dermatol. 17, 243-277 (2001).
    • (2001) Adv. Dermatol. , vol.17 , pp. 243-277
    • Richard, G.1
  • 7
    • 0032546033 scopus 로고    scopus 로고
    • Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa
    • Brobby, G.W., Müller-Myhsok, B. & Horstmann, R.D. Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa. N. Engl. J. Med. 338, 548-550 (1998).
    • (1998) N. Engl. J. Med. , vol.338 , pp. 548-550
    • Brobby, G.W.1    Müller-Myhsok, B.2    Horstmann, R.D.3
  • 9
    • 0034098926 scopus 로고    scopus 로고
    • Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
    • Rabionet, R. et al. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. Hum. Genet. 106, 40-44 (2000).
    • (2000) Hum. Genet. , vol.106 , pp. 40-44
    • Rabionet, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.