Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency
- 6 January 1969
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 34 (1), 77-83
- https://doi.org/10.1016/0006-291x(69)90531-2
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Muscle Phosphofructokinase DeficiencyArchives of Neurology, 1967
- Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosisBiochemical and Biophysical Research Communications, 1965
- The hydrogen ion concentrations and erythrocyte glycolysisBiochemical and Biophysical Research Communications, 1964
- IMMUNOCHEMICAL PROPERTIES OF LACTATE DEHYDROGENASE ISOZYMESAnnals of the New York Academy of Sciences, 1963
- ERYTHROCYTE METABOLISM. VI. SEPARATION OF ERYTHROCYTE ENZYMES FROM HEMOGLOBIN*Journal of Clinical Investigation, 1962