Rare causes of hereditary iron overload
- Author
- PONKA, Prem1
[1] Lady Davis Institute for Medical Research of the Jewish General Hospital, and the Departments of Physiology and Medicine, McGill University, Montreal, Quebec, Canada - Issue title
- Hereditary disorders of iron metabolism
- Author (monograph)
- KUSHNER, James P (Editor)1
[1] Division of Hematology, University of Utah School of Medicine, 50 N Medical Dr, Salt Lake City, UT 84132, United States - Source
Seminars in hematology. 2002, Vol 39, Num 4, pp 249-262, 14 p ; ref : 74 ref
- CODEN
- SEHEA3
- ISSN
- 0037-1963
- Scientific domain
- Hematology
- Publisher
- Elsevier, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Animal Article synthèse Classification Fer Ferroprotéine Gène Heme oxygenase (decyclizing) Homme Hémochromatose Mutation Pathogénie Protein-tyrosine kinase Récepteur biologique Transferrine Protein-kinase PANK2 Protéine IRP2 Enzyme Enzymopathie Génétique Maladie héréditaire Métabolisme pathologie Oxidoreductases Transferases
- Keyword (en)
- Animal Review Classification Iron Ferroprotein Gene Heme oxygenase (decyclizing) Human Hemochromatosis Mutation Pathogenesis Protein-tyrosine kinase Biological receptor Transferrin Enzyme Enzymopathy Genetics Genetic disease Metabolic diseases Oxidoreductases Transferases
- Keyword (es)
- Animal Artículo síntesis Clasificación Hierro Ferroproteina Gen Heme oxygenase (decyclizing) Hombre Hemocromatosis Mutación Patogenia Protein-tyrosine kinase Receptor biológico Transferrina Enzima Enzimopatía Genética Enfermedad hereditaria Metabolismo patología Oxidoreductases Transferases
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22E Other metabolic disorders / 002B22E03 Metals (hemochromatosis...)
- Discipline
- Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 13992261
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1053/shem.2002.35638 
https://dx.doi.org/10.1053/shem.2002.35638
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