Absence of β-Globin Synthesis and Excess of α-Globin Synthesis in Homozygous β-Thalassaemic Subjects from the Ferrara Region
- 1 January 1968
- journal article
- letter
- Published by Springer Nature in Nature
- Vol. 217 (5125), 259-260
- https://doi.org/10.1038/217259a0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Homozygous βδ Thalassaemia (βδ Microcythaemia)Nature, 1966
- Electron Microscope Observations on the Free Protein and the Protein-Polysaccharide Complex of Bovine Synovial FluidNature, 1965
- An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)Nature, 1965
- Amino Acids: Incorporation into α- and β-Chains of Hemoglobin by Normal and Thalassemic ReticulocytesScience, 1964
- Hemoglobins A and F: Formation in Thalassemia and Other Hemolytic AnemiasScience, 1964
- Current Concepts of the Genetics of the ThalassemiasPublished by Cold Spring Harbor Laboratory ,1964
- THE TURNOVER OF HEMOGLOBINS A, F, AND A2 IN THE PERIPHERAL BLOOD OF THREE PATIENTS WITH THALASSEMIA*JCI Insight, 1963
- The preparation and properties of haemoglobin αA, a haemoglobin consisting of αA-polypeptide chainsJournal of Molecular Biology, 1962
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine ContentJournal of the American Chemical Society, 1958