Molecular characterization of six unrelated Italian patients affected by pyrimidine 5′‐nucleotidase deficiency
Open Access
- 21 August 2003
- journal article
- website
- Published by Wiley in British Journal of Haematology
- Vol. 122 (5) , 847-851
- https://doi.org/10.1046/j.1365-2141.2003.04532.x
Abstract
The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.Keywords
This publication has 23 references indexed in Scilit:
- Iron Status and HFE Genotype in Erythrocyte Pyruvate Kinase Deficiency: Study of Italian CasesBlood Cells, Molecules, and Diseases, 2001
- Heterogeneity of hemochromatosis in ItalyGastroenterology, 1998
- Assignment of the human gene for uridine 5?-monophosphate phosphohydrolase (UMPH2) to the long arm of chromosome 17Annals of Human Genetics, 1986
- Erythrocyte Pyrimidine 5‘‐Nucleotidase DeficiencyScandinavian Journal of Haematology, 1983
- Isozymes of rodent 5?-nucleotidase: evidence for two independent structural loci Umph-1 and Umph-2Annals of Human Genetics, 1983
- A Case of Hemolytic Anemia Due to Erythrocyte Pyrimidine 5′-Nucleotidase DeficiencyActa Haematologica, 1981
- Additional Data from Two Kindreds with Genetically Induced Deficiencies of Erythrocyte Pyrimidine NucleotidaseActa Haematologica, 1980
- Hereditary Hemolytic Anemia with Human Erythrocyte Pyrimidine 5′-Nucleotidase DeficiencyJournal of Clinical Investigation, 1974
- Electrophoretic analysis of the major polypeptides of the human erythrocyte membraneBiochemistry, 1971
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970