[Pyruvate kinase deficiency].
Copyright policy )[Pyruvate kinase deficiency].
PK deficiency is the most common and well characterized erythroenzymopathy in the Embden-Meyerhof glycolytic pathway associated with hereditary hemolytic anemia. History of discovery, clinical features, biochemical studies, as well as recent studies on molecular level were reviewed, with a stress on our own studies. As reference materials, Tables 2 and 3 are attached.
Electrophoresis, Anemia, Hemolytic, Erythrocytes, Adolescent, Pyruvate Kinase, Cell Differentiation, DNA, Anemia, Hemolytic, Congenital Nonspherocytic, Anemia, Hemolytic, Congenital, Isoenzymes, Chromosomes, Human, Pair 1, Humans, Female
Electrophoresis, Anemia, Hemolytic, Erythrocytes, Adolescent, Pyruvate Kinase, Cell Differentiation, DNA, Anemia, Hemolytic, Congenital Nonspherocytic, Anemia, Hemolytic, Congenital, Isoenzymes, Chromosomes, Human, Pair 1, Humans, Female
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