Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.
Open Access
- 1 December 1968
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 5 (4) , 292-297
- https://doi.org/10.1136/jmg.5.4.292
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Abnormal Haem Binding and Globin SH Group Blockade in Unstable HaemoglobinsNature, 1968
- Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)Nature, 1967
- Hemoglobin Gun Hill: Deletion of Five Amino Acid Residues and Impaired Heme-Globin BindingScience, 1967
- Haemoglobin Genova: β28 (B10) Leucine→ProlineNature, 1967
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body AnaemiaNature, 1966
- Human HaemoglobinsJournal of Medical Genetics, 1965
- Hereditary Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- Human haemoglobin A2Biochimica et Biophysica Acta, 1962
- TRIS Buffer for the Demonstration of Haemoglobin A2by Paper ElectrophoresisJournal of Clinical Pathology, 1959