Advances in hereditary red cell enzyme anomalies
- 1 August 1979
- journal article
- review article
- Published by Springer Nature in Human Genetics
- Vol. 50 (1) , 1-27
- https://doi.org/10.1007/bf00295584
Abstract
No abstract availableKeywords
This publication has 129 references indexed in Scilit:
- Congenital Methemoglobin- Reductase (Cytochrome b5 Reductase) Deficiency Associated with Mental Retardation in a Spanish GirlActa Haematologica, 1978
- NADPH-flavin reductase in human erythrocytes and the reduction of methemoglobin through flavin by the enzymeBiochemical and Biophysical Research Communications, 1977
- Diphosphoglycerate mutase and 2,3-diphosphoglycerate phosphatase activities of red cells: Comparative electrophoretic studyBiochemical and Biophysical Research Communications, 1973
- Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic diseaseThe Journal of Pediatrics, 1973
- Presence of red cell type NADH-methemoglobin reductase (NADH-diaphorase) in human non erythroid cellsBiochemical and Biophysical Research Communications, 1972
- Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiencyBiochemical and Biophysical Research Communications, 1969
- Electrophoretic abnormality in triosephosphate isomerase deficiencyBiochemical and Biophysical Research Communications, 1968
- Red cell phosphoglycerate kinase deficiencyBiochemical and Biophysical Research Communications, 1968
- Hexokinasemangel in Blutzellen bei einer Sippe mit familiärer Panmyelopathie (Typ Fanconi)Klinische Wochenschrift, 1965
- Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosisBiochemical and Biophysical Research Communications, 1965