G6PD-Puerto Limón: A new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia
- 1 December 1982
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 62 (2) , 110-112
- https://doi.org/10.1007/bf00282295
Abstract
A new glucose-6-phosphate dehydrogenase (G6PD) variant with total deficiency associated with congenital nonspherocytic hemolytic anemia was found in a Costa Rican family. The study of the partially purified enzyme revealed thermal instability, increased G6P affinity, abnormal pH optimum, increased utilization of analogues, and a chromatographic behavior that differs from all the variants previously described. Thus, this new variant was designated G6PD Puerto Limón.Keywords
This publication has 9 references indexed in Scilit:
- Human erythrocyte glucose 6-phosphate dehydrogenase: structure and function in normal and mutant subjects.1978
- Human glucose‐6‐phosphate dehydrogenase variants: a supplementary tabulationAnnals of Human Genetics, 1978
- Human glucose-6-phosphate dehydrogenase variants: a supplementary tabulationAnnals of Human Genetics, 1973
- Treatment of haemoglobinopathies and allied disorders. Report of a WHO Scientific Group.1972
- A simple and rapid dye test for glucose-6-phosphate dehydrogenase deficiency for routine use.1970
- Standardization of procedures for the study of glucose-6-phosphate dehydrogenase. Report of a WHO Scientific Group.1967
- GLUCOSE 6-PHOSPHATE DEHYDROGENASE OF HUMAN ERYTHROCYTES .I. PURIFICATION AND CHARACTERIZATION OF NORMAL (B+) ENZYME1966
- The Methemoglobin Reduction Test for Primaquine-Type Sensitivity of ErythrocytesJAMA, 1962