Aminolevulinate Inhibition of Human Coproporphyrinogen Oxidase clarifies Coproporphyrin III Accumulation in Porphyrias
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Porphyrias are inherited or acquired disorders of heme biosynthesis characterized by heme deficiency and accumulation of toxic intermediates. In δ-aminolevulinic acid dehydratase deficiency porphyria (ALADP), patients consistently present elevated urinary δ-... ...