Athens Variant of Glucose-6-Phosphate Dehydrogenase
- 18 August 1967
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 157 (3790), 831-833
- https://doi.org/10.1126/science.157.3790.831
Abstract
A variant of glucose-6-phosphate dehydrogenase (G6PD), characterized by slower than normal electrophoretic migration and associated with mild deficiency of G6PD in the red cells, was detected in two unrelated Greek males. Electrophoretic, chromatographic, and enzymologic study indicated that the new mutant is structurally different from normal G6PD (B+) and from the Mediterranean variant associated with red-cell enzyme deficiency (B-). Convincing electrophoretic separation of the new variant from the normal B+ and the Mediterranean B- enzymes was achieved only by detailed electrophoretic study in different buffer systems and conditions.This publication has 4 references indexed in Scilit:
- Negro Variant of Glucose-6-Phosphate Dehydrogenase Deficiency (A - ) in ManScience, 1967
- A new glucose‐6‐phosphate dh/ehydrogenase mutant (Tel‐Hashomer Mutant)*Annals of Human Genetics, 1964
- Erythrocyte Glucose-6-Phosphate Dehydrogenase in Caucasians: New Inherited VariantScience, 1964
- Functionally Abnormal Glucose-6-Phosphate DehydrogenasesCold Spring Harbor Symposia on Quantitative Biology, 1964