메뉴 건너뛰기




Volumn 34, Issue 4, 1997, Pages 275-278

Global prevalence of putative haemochromatosis mutations

Author keywords

Haemochromatosis; HLA H; North European Celtic populations

Indexed keywords

ASPARTIC ACID; CYSTEINE; HISTIDINE; HLA ANTIGEN; RESTRICTION ENDONUCLEASE; TYROSINE;

EID: 0030923653     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.4.275     Document Type: Article
Times cited : (716)

References (12)
  • 3
    • 0018671569 scopus 로고
    • Serum ferritin as a possible marker of the haemochromatosis allele
    • Beaumont C, Simon M, Fauchet R, et al. Serum ferritin as a possible marker of the haemochromatosis allele. N Engl J Med 1979;301:169-74.
    • (1979) N Engl J Med , vol.301 , pp. 169-174
    • Beaumont, C.1    Simon, M.2    Fauchet, R.3
  • 7
    • 0025740120 scopus 로고
    • Screening for haemochromatosis: Prevalence among Danish blood donors
    • Wiggers P, Dalhøj J, Kiær H, et al. Screening for haemochromatosis: prevalence among Danish blood donors. J Intern Med 1991;230:265-70.
    • (1991) J Intern Med , vol.230 , pp. 265-270
    • Wiggers, P.1    Dalhøj, J.2    Kiær, H.3
  • 8
    • 9344224529 scopus 로고    scopus 로고
    • A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    • Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;13:399-409.
    • (1996) Nat Genet , vol.13 , pp. 399-409
    • Feder, J.N.1    Gnirke, A.2    Thomas, W.3
  • 10
    • 0030221927 scopus 로고    scopus 로고
    • Mutation analysis in hereditary haemochromatosis
    • Beutler E, Gelbart T, West C, et al. Mutation analysis in hereditary haemochromatosis. Blood Cells Mol Dis 1996;22:187-94.
    • (1996) Blood Cells Mol Dis , vol.22 , pp. 187-194
    • Beutler, E.1    Gelbart, T.2    West, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.