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Hereditary Tyrosinemia and the Heme Biosynthetic Pathway. PROFOUND INHIBITION OF δ-AMINOLEVULINIC ACID DEHYDRATASE ACTIVITY BY SUCCINYLACETONE

Succinylacetone (4,6-dioxoheptanoic acid) is an abnormal metabolite produced in patients with hereditary tyrosinemia as a consequence of an inherited deficiency of fumarylacetoacetate hydrolase. It is known that patients with this hereditary disease excrete excessive amounts of δ-aminolevulinic acid...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Sassa, Shigeru, Kappas, Attallah
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1983
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC436912/
https://ncbi.nlm.nih.gov/pubmed/6826727
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