An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.

Uroporphyrinogen decarboxylase activity was measured in liver and erythrocytes of normal subjects and in patients with porphyria cutanea tarda and their relatives. In patients with porphyria cutanea tarda, hepatic uroporphyrinogen decarboxylase activity was significantly reduced (mean 0.43 U/mg prot...

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Dades bibliogràfiques

Publicat a:	J Clin Invest
Autors principals:	Kushner, J P, Barbuto, A J, Lee, G R
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1976
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC333275/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/993332/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108560
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