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Volumn 59, Issue 1, 2001, Pages 37-41

The molecular basis of cystic fibrosis in South Africa

Author keywords

African populations; CFTR mutations; Cystic fibrosis; Haplotypeanalysis

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 0035169491     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.590106.x     Document Type: Article
Times cited : (31)

References (26)
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  • 11
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  • 14
    • 0032796106 scopus 로고    scopus 로고
    • Cystic fibrosis patients with the 3272 - 26A → G mutation have mild disease, leaky alternative mRNA splicing and CFTR protein at the cell membrane
    • (1999) Human Mutation , vol.14 , pp. 133-144
    • Beck, S.1    Penque, D.2    Garcia, S.3
  • 15
    • 0026780584 scopus 로고
    • Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions
    • (1992) Genomics , vol.13 , pp. 770-776
    • Fanen, P.1    Ghanem, N.2    Vidaud, M.3
  • 17
    • 0027234275 scopus 로고
    • Analysis of the 27 exons and flanking regions of the cystic fibrosis gene, 40 different mutations account for 91.2% of the mutant alleles in Southern France
    • (1993) Hum Mol Genet , vol.2 , Issue.8 , pp. 1209-1213
    • Claustres, M.1    Laussel, M.2    Desgeorges, M.3
  • 20
    • 0030759984 scopus 로고    scopus 로고
    • Analysis of 22 cystic fibrosis mutations in 62 Patients from the Flanders, Belgium, reveals a high prevalence of the Nordic mutation 394delTT
    • (1997) Hum Mutat , vol.10 , pp. 236-238
    • Messiaen, L.1    Van Loon, C.2    Rossau, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.