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Genetic Heterogeneity Underlies Juvenile Hemochromatosis Phenotype: Analysis of Three Families of Northern Greek Origin

  • Published:2002-09 Issue:2 Volume:29 Page:168-173
  • ISSN:1079-9796
  • Container-title:Blood Cells, Molecules, and Diseases
  • language:en
  • Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Papanikolaou G.,Papaioannou M.,Politou M.,Vavatsi N.,Kioumi A.,Tsiatsiou P.,Marinaki P.,Loukopoulos D.,Christakis J.I.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference21 articles.

1. Prevalence of hemochromatosis among 11.065 presumably healthy blood donors;Edwards;N. Engl. J. Med.,1988

2. Hereditary hemochromatosis: Phenotypic expression of the disease;Cartwright;N. Engl. J. Med.,1979

3. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat. Genet.,1996

4. Mutation analysis in hereditary hemochromatosis;Beutler;Blood Cells Mol. Dis.,1996

5. Mutation analysis of the HLA-H gene in Italian hemochromatosis patients;Carella;Am. J. Hum. Genet.,1997

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