Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX

Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX

A variant form of phosphorylase kinase deficiency is described and studied using erythrocyte and leukocyte enzyme activities.

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Bibliographische Detailangaben
Veröffentlicht in:Journal of inherited metabolic disease 1987-06, Vol.10 (2), p.119-127
Hauptverfasser: Bashan, N., Potashnik, R., Ehrlich, T., Moses, S. W.
Format: Artikel
Sprache:eng
Schlagworte:
Biological and medical sciences
Carbohydrates (enzymatic deficiencies). Glycogenosis
Enzyme Activation
Errors of metabolism
Erythrocytes - enzymology
Glycogen Storage Disease - classification
Glycogen Storage Disease - enzymology
Glycogen Storage Disease - genetics
Humans
Infant
Kinetics
Leukocytes - enzymology
Male
Medical sciences
Metabolic diseases
Mutation
Phosphorylase Kinase - blood
Phosphorylase Kinase - deficiency
Phosphorylase Kinase - genetics
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Beschreibung
Zusammenfassung:A variant form of phosphorylase kinase deficiency is described and studied using erythrocyte and leukocyte enzyme activities.
ISSN:0141-8955
1573-2665
DOI:10.1007/BF01800035