Clinical and Molecular Aspects of Juvenile Hemochromatosis in Saguenay–Lac-Saint-Jean (Quebec, Canada)
- 29 February 2000
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 26 (1) , 10-14
- https://doi.org/10.1006/bcmd.2000.0271
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada)British Journal of Haematology, 2000
- Juvenile Hemochromatosis Locus Maps to Chromosome 1qAmerican Journal of Human Genetics, 1999
- Hemochromatosis in Ireland and HFEBlood Cells, Molecules, and Diseases, 1998
- Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.Journal of Medical Genetics, 1998
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996
- Autosomal recessive disorders in Saguenay‐Lac‐Saint‐Jean (Quebec, Canada): a study of inbreedingAnnals of Human Genetics, 1996
- A prevalence and fertility study of haemochromatosis in Saguenay-Lac-Saint-JeanAnnals of Human Biology, 1993
- Hemochromatosis and pyruvate kinase deficiencyAnnals of Hematology, 1991
- Hereditary Disorders in Saguenay-Lac-St-Jean (Quebec, Canada)Human Heredity, 1991
- Case 25-1983New England Journal of Medicine, 1983