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Volumn 29, Issue 1, 2002, Pages 41-47

Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; HFE PROTEIN, HUMAN; HLA ANTIGEN CLASS 1; MEMBRANE PROTEIN;

EID: 0002878060     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.2002.0536     Document Type: Article
Times cited : (56)

References (20)
  • 8
    • 0037132786 scopus 로고    scopus 로고
    • Penetrance of 845G A (C282Y) HFE hereditary hemochromatosis mutation in the USA
    • E. Beutler V. Felitti J Koziol N.J. Ho T. Gelbart Penetrance of 845G A (C282Y) HFE hereditary hemochromatosis mutation in the USA Lancet 359 2002 211 218
    • (2002) Lancet , vol.359 , pp. 211-218
    • Beutler, E.1    Felitti, V.2    Koziol, J3    Ho, N.J.4    Gelbart, T.5
  • 10
    • 0033817852 scopus 로고    scopus 로고
    • A common intron 3 mutation (IVS3 -48c→g) leads to misdiagnosis of the c.845G→A (C282Y) HFE gene mutation
    • E. Beutler T. Gelbart A common intron 3 mutation (IVS3 -48c→g) leads to misdiagnosis of the c.845G→A (C282Y) HFE gene mutation Blood Cells Mol. Dis 26 2000 229 233
    • (2000) Blood Cells Mol. Dis , vol.26 , pp. 229-233
    • Beutler, E.1    Gelbart, T.2
  • 11
    • 0032775931 scopus 로고    scopus 로고
    • Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis [letter]
    • G.P. Jeffrey S. Chakrabarti R.A. Hegele P.C. Adams Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis [letter] Nature Genet 22 1999 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
  • 13
    • 0014687735 scopus 로고
    • Caucasian Genes in American Negroes
    • T. Reed Caucasian Genes in American Negroes Science 165 1966 762 768
    • (1966) Science , vol.165 , pp. 762-768
    • Reed, T.1
  • 16
    • 85120205221 scopus 로고    scopus 로고
    • Beutler, E., Gelbart, T., West, C., Lee, P., Adams, M., Blackstone, R., Pockros, P., Kosty, M., Venditti, C. P., Phatak, P. D., Seese, N. K., Chorney, K. A., Ten Elshof, A. E., Gerhard, G. S., and Chorney, M: Mutation analysis in hereditary hemochromatosis. Blood Cells, Mol. Dis.22, 187–194.
  • 17
    • 0030827084 scopus 로고    scopus 로고
    • The significance of the 187G (H63D) mutation in hemochromatosis [letter; comment]
    • E. Beutler The significance of the 187G (H63D) mutation in hemochromatosis [letter; comment] Am. J. Hum. Genet 61 1997 762 764
    • (1997) Am. J. Hum. Genet , vol.61 , pp. 762-764
    • Beutler, E.1
  • 19
    • 0034572933 scopus 로고    scopus 로고
    • Iron homeostasis: Insights from genetics and animal models
    • N.C. Andrews Iron homeostasis: Insights from genetics and animal models Nature Rev. Genet 1 2000 208 217
    • (2000) Nature Rev. Genet , vol.1 , pp. 208-217
    • Andrews, N.C.1
  • 20
    • 0033848697 scopus 로고    scopus 로고
    • EASL International Consensus Conference on Haemochromatosis
    • P. Adams P. Brissot L.W. Powell EASL International Consensus Conference on Haemochromatosis J. Hepatol 33 2000 485 504
    • (2000) J. Hepatol , vol.33 , pp. 485-504
    • Adams, P.1    Brissot, P.2    Powell, L.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.