Hypochromie der Erythrozyten bei heterozygotem Hämoglobin E (β26 Glu→Lys)
- 1 January 1976
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 56 (5) , 276-284
- https://doi.org/10.1159/000207948
Abstract
A family from south-western Germany with 9 heterozygous carriers of haemoglobin E (β26 Glu-Lys) is presented. The abnormal haemoglobin has been identified by different electrophoretic techniques and fingerprint analysis. In contrast to earlier observations, haemoglobin E is even in heterozygous carriers associated with erythrocytic hypochromia with MCH values from 23.6 to 26.2 pg. As an explanation for the hypochromia a decreased haemoglobin synthesis is supposed.Keywords
This publication has 4 references indexed in Scilit:
- EFFECT OF IRON DEFICIENCY ON LEVELS OF HEMOGLOBINS A2 AND E1968
- The First Instance of Hemoglobin E in a Japanese FamilyProceedings of the Japan Academy, 1964
- Abnormal human haemoglobins VI. The chemical difference between haemoglobins A and EBiochimica et Biophysica Acta, 1961
- PROTEIN COAGULATION AND ITS REVERSALThe Journal of general physiology, 1930