In inherited porphyrias, lead intoxication is a toxogenetic disorder

1. 1. δ-Aminolevulinic acid dehydratase (ALA-D), blood lead and several enzymes and metabolites of the heme biosynthetic pathway were measured in a number of symptomatic porphyric patients, 22 with acute intermittent porphyria, three with hereditary hepatic coproporphyria, 10 with hereditary porphyr...

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Detalles Bibliográficos
Autores principales:	Del C. Batlle, A.M., Fukuda, H., Parera, V.E., Wider, E., Stella, A.M.
Formato:	JOUR
Materias:	lead porphobilinogen synthase acute intermittent porphyria blood blood and hemopoietic system congenital disorder congenital erythropoietic porphyria erythropoietic protoporphyria etiology human intoxication lead poisoning porphyria porphyria cutanea tarda priority journal review Heme Humans Lead Lead Poisoning Porphobilinogen Synthase Porphyrias
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_0020711X_v19_n8_p717_DelCBatlle
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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