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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Bibliographic Details

Published in:	J Clin Invest
Main Authors:	Kushner, J P, Barbuto, A J, Lee, G R
Format:	Artigo
Language:	Inglês
Published:	American Society for Clinical Investigation 1976
Subjects:	Research Article
Online Access:	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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