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Volumn 54, Issue 4, 2005, Pages 567-568

Identification of ferroportin disease in the Indian subcontinent [8]

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; FERROPORTIN 1; HFE PROTEIN;

EID: 15444380100     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2004.060988     Document Type: Letter
Times cited : (22)

References (9)
  • 1
    • 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;13:399-408.
    • (1996) Nat Genet , vol.13 , pp. 399-408
    • Feder, J.N.1    Gnirke, A.2    Thomas, W.3
  • 2
    • 1442306702 scopus 로고    scopus 로고
    • Non-HFE hemochromatosis
    • Pietrangelo A. Non-HFE hemochromatosis. Hepatology 2004;39:21-9.
    • (2004) Hepatology , vol.39 , pp. 21-29
    • Pietrangelo, A.1
  • 3
  • 4
    • 1642513739 scopus 로고    scopus 로고
    • Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major
    • Kour G, Rapthap CC, Xavier M, et al. Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major. Natl Med J India 2003;16:309-10.
    • (2003) Natl Med J India , vol.16 , pp. 309-310
    • Kour, G.1    Rapthap, C.C.2    Xavier, M.3
  • 5
    • 1642480107 scopus 로고    scopus 로고
    • Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India
    • Thakur V, Guptan RC, Hashmi AZ, et al. Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India. J Gastroenterol Hepatol 2004;19:86-90.
    • (2004) J Gastroenterol Hepatol , vol.19 , pp. 86-90
    • Thakur, V.1    Guptan, R.C.2    Hashmi, A.Z.3
  • 6
    • 0037100517 scopus 로고    scopus 로고
    • Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis
    • Wallace DF, Pedersen P, Dixon JL, et al. Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis. Blood 2002;100:692-4.
    • (2002) Blood , vol.100 , pp. 692-694
    • Wallace, D.F.1    Pedersen, P.2    Dixon, J.L.3
  • 7
    • 0037100382 scopus 로고    scopus 로고
    • Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)
    • Devalia V, Carter K, Walker AP, et al. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3). Blood 2002;100:695-7.
    • (2002) Blood , vol.100 , pp. 695-697
    • Devalia, V.1    Carter, K.2    Walker, A.P.3
  • 8
    • 0037100383 scopus 로고    scopus 로고
    • A valine deletion of ferroportin 1: A common mutation in hemochromastosis type 4
    • Roetto A, Merryweather-Clarke AT, Daraio F, et al. A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4. Blood 2002;100:733-4.
    • (2002) Blood , vol.100 , pp. 733-734
    • Roetto, A.1    Merryweather-Clarke, A.T.2    Daraio, F.3
  • 9
    • 18744400781 scopus 로고    scopus 로고
    • Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
    • Cazzala M, Cremonesi L, Papaioannou M, et al. Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3). Br J Haematol 2002;119:539-46.
    • (2002) Br J Haematol , vol.119 , pp. 539-546
    • Cazzala, M.1    Cremonesi, L.2    Papaioannou, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.