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Volumn 7, Issue 2, 2003, Pages 155-158

HFE alleles in an Irish cystic fibrosis population

Author keywords

[No Author keywords available]

Indexed keywords

HFE PROTEIN;

EID: 0037477694     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/109065703322146876     Document Type: Article
Times cited : (12)

References (26)
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  • 8
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    • Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers of the French CF Registry
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    • Feingold, J.1    Guilloud-Bataille, M.2
  • 9
    • 0032775931 scopus 로고    scopus 로고
    • Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis
    • JEFFREY, G.P., CHAKRABARTI, S., HEGELE, R.A., and ADAMS, P.C. (1999). Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis. Nature Genet. 22, 325-326.
    • (1999) Nature Genet. , vol.22 , pp. 325-326
    • Jeffrey, G.P.1    Chakrabarti, S.2    Hegele, R.A.3    Adams, P.C.4
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    • Celtic origin of the C282Y mutation of hemochromatosis
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  • 19
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    • Modulation of disease severity in cystic fibrosis transmembrane conductance regulator (CFTR) deficient mice by a secondary genetic factor
    • ROZMAHEL, R., WILSCHANSKI, M., MATIN, A., PLYTE, S., OLIVER, M., AUERBACH, W., MOORE, A., FORSTNER, J., DURIE, P., NADEAU, J., et al. (1996). Modulation of disease severity in cystic fibrosis transmembrane conductance regulator (CFTR) deficient mice by a secondary genetic factor. Nature Genet. 12, 280-287.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.