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Volumn 100, Issue 2, 1997, Pages 279-283

Cystic fibrosis in Lebanon: Distribution of CFTR mutations among Arab communities

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 1842407140     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050505     Document Type: Article
Times cited : (58)

References (10)
  • 1
    • 0014460883 scopus 로고
    • Cystic fibrosis of the pancreas
    • Bitard J, Idriss H (1969) Cystic fibrosis of the pancreas. Leb Med J 22:181-185
    • (1969) Leb Med J , vol.22 , pp. 181-185
    • Bitard, J.1    Idriss, H.2
  • 2
    • 0029758296 scopus 로고    scopus 로고
    • CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France
    • Claustres M, Desgeorges M, Moine P, Morral N, Extivill X (1996) CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France. Hum Genet 98 : 336-344
    • (1996) Hum Genet , vol.98 , pp. 336-344
    • Claustres, M.1    Desgeorges, M.2    Moine, P.3    Morral, N.4    Extivill, X.5
  • 5
    • 0028140183 scopus 로고
    • Exon 9 of the CFTR gene: Splice site haplotypes and cystic fibrosis mutations
    • Dork T, Fislage R, Neumann T, Wulf B, Tümmler B (1994) Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations. Hum Genet 93:67-73
    • (1994) Hum Genet , vol.93 , pp. 67-73
    • Dork, T.1    Fislage, R.2    Neumann, T.3    Wulf, B.4    Tümmler, B.5
  • 8
    • 0026503640 scopus 로고
    • Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease
    • Shoshani T, Augarten A, Gazit E, Bashan N, Yahav Y, Rivlin Y, Tal A, Seret H, Yaar L, Kerem E, Kerem B-S (1992) Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease. Am J Hum Genet 50:222-228
    • (1992) Am J Hum Genet , vol.50 , pp. 222-228
    • Shoshani, T.1    Augarten, A.2    Gazit, E.3    Bashan, N.4    Yahav, Y.5    Rivlin, Y.6    Tal, A.7    Seret, H.8    Yaar, L.9    Kerem, E.10    Kerem, B.-S.11
  • 9
    • 0028265203 scopus 로고
    • Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21
    • Shoshani T, Augarten A, Yahav J, Gazit E. Kerem B (1994) Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21. Hum Mol Genet 3:657-658
    • (1994) Hum Mol Genet , vol.3 , pp. 657-658
    • Shoshani, T.1    Augarten, A.2    Yahav, J.3    Gazit, E.4    Kerem, B.5
  • 10
    • 0028033069 scopus 로고
    • Population variation of common cystic fibrosis mutations
    • The Cystic Fibrosis Genetic Analysis Consortium (1994) Population variation of common cystic fibrosis mutations. Hum Mutat 4:167-177
    • (1994) Hum Mutat , vol.4 , pp. 167-177


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.