Inheritance of two HFE mutations in African Americans: Cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency

This publication has 32 references indexed in Scilit:

• Transferrin Receptor-2 (TFR2) Mutation Y250X in Alabama Caucasian and African American Subjects with and without Primary Iron Overload
  Blood Cells, Molecules, and Diseases, 2001
• Iron overload in African Americans
  Published by Cambridge University Press (CUP) ,2000
• Human leukocyte antigen (HLA) association and typing in hemochromatosis
  Published by Cambridge University Press (CUP) ,2000
• Correlation Between Genotype and Phenotype in Hereditary Hemochromatosis: Analysis of 61 Cases
  Blood Cells, Molecules, and Diseases, 1997
• HLA-H Mutations in the Ashkenazi Jewish Population
  Blood Cells, Molecules, and Diseases, 1997
• Global prevalence of putative haemochromatosis mutations.
  Journal of Medical Genetics, 1997
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• Hereditary hemochromatosis
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1996
• HLA Phenotype and Haplotype Frequencies in the Cantabria (Middle North Spain) Population
  Human Heredity, 1991
• DIETARY IRON OVERLOAD PERSISTS IN RURAL SUB-SAHARAN AFRICA
  The Lancet, 1986