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Volumn 155, Issue 10, 2011, Pages 2453-2458

Did the GJB2 35delG mutation originate in Iran?

Author keywords

35delG; ARNSHL; GJB2; Iran

Indexed keywords

GUANINE;

EID: 80053122535     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34225     Document Type: Article
Times cited : (13)

References (21)
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    • A gene responsible for a dominant form of neurosensory nonsyndromic deafness maps to the NSRD1 recessive deafness gene interval
    • Chaib H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C. 1994. A gene responsible for a dominant form of neurosensory nonsyndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum Mol Genet 3: 2219-2222.
    • (1994) Hum Mol Genet , vol.3 , pp. 2219-2222
    • Chaib, H.1    Lina-Granade, G.2    Guilford, P.3    Plauchu, H.4    Levilliers, J.5    Morgon, A.6    Petit, C.7
  • 10
    • 17844395222 scopus 로고    scopus 로고
    • The 35delG Mutation in the Connexin 26 Gene (GJB2) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece, GENETIC TESTING, copy; Mary Ann Liebert, Inc. 9: 20-25.
    • Lucotte G, Diéterlen F. 2005. The 35delG Mutation in the Connexin 26 Gene (GJB2) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece, GENETIC TESTING, © Mary Ann Liebert, Inc. 9: 20-25.
    • (2005)
    • Lucotte, G.1    Diéterlen, F.2
  • 14
    • 0033812813 scopus 로고    scopus 로고
    • Connexin26 mutations associated with nonsyndromic hearing loss
    • Park HJ, Hahn SH, Chun YM, Park K, Kim HN. 2000. Connexin26 mutations associated with nonsyndromic hearing loss. Laryngoscope 110: 1535-1538.
    • (2000) Laryngoscope , vol.110 , pp. 1535-1538
    • Park, H.J.1    Hahn, S.H.2    Chun, Y.M.3    Park, K.4    Kim, H.N.5
  • 16
    • 0035081453 scopus 로고    scopus 로고
    • A seminested PCR test for simultaneous detection of two common mutations (35delG and 167delT) in the connexin-26 gene
    • Simsek M, Al-Wardy N, Al-Khabory M. 2001a. A seminested PCR test for simultaneous detection of two common mutations (35delG and 167delT) in the connexin-26 gene. Mol Diagn 6: 63-67.
    • (2001) Mol Diagn , vol.6 , pp. 63-67
    • Simsek, M.1    Al-Wardy, N.2    Al-Khabory, M.3
  • 18
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    • Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians
    • Tekin M, Akar N, Cin S, Blanton SH, Xia XJ, Liu XZ, Nance WE, Pandya A. 2001. Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians. Hum Genet 108: 385-389.
    • (2001) Hum Genet , vol.108 , pp. 385-389
    • Tekin, M.1    Akar, N.2    Cin, S.3    Blanton, S.H.4    Xia, X.J.5    Liu, X.Z.6    Nance, W.E.7    Pandya, A.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.