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Volumn 2002, Issue 339, 2002, Pages 39-43

Hemochromatosis and primary iron overload;Hémochromatoses et surcharges primitives en fer

Author keywords

H mochromatosis; Iron; Mutation; Tissu overload

Indexed keywords


EID: 16844381961     PISSN: 03389898     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0338-9898(02)80139-1     Document Type: Article
Times cited : (1)

References (16)
  • 2
    • 0030827084 scopus 로고    scopus 로고
    • The significance of the 187G (H63D) mutation in hemochromatosis
    • Beutler E., The significance of the 187G (H63D) mutation in hemochromatosis, Am. J. Hum. Genet. 61 (1997) 762-764.
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 762-764
    • Beutler, E.1
  • 14
    • 0016240373 scopus 로고
    • Idiopathic haemochromatosis, An autosomal recessive disease
    • Saddi R., Feingold J., Idiopathic haemochromatosis, An autosomal recessive disease, Clin. Genet. 5 (1974) 234-241.
    • (1974) Clin. Genet. , vol.5 , pp. 234-241
    • Saddi, R.1    Feingold, J.2
  • 15
    • 0017158302 scopus 로고
    • Association of HLA-A3 antigens with idiopathic haemochromatosis
    • Simon M., Bourel M., Fauchet R., Genetet B., Association of HLA-A3 antigens with idiopathic haemochromatosis, GUT 17 (1976) 332-334.
    • (1976) GUT , vol.17 , pp. 332-334
    • Simon, M.1    Bourel, M.2    Fauchet, R.3    Genetet, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.