Abstract
A method for measuring uroporphyrinogen decarboxylase activity is described. The method measures uroporphyrinogen decarboxylase activity equally sensitively using either uroporphyrinogen I or III as substrate.Using this method uroporphyrinogen decarboxylase activity was measured in the erythrocytes and enriched reticulocytes of healthy normal persons as well as in rat liver homogenates.
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