Acute porphyrias in the Argentinean population: a review.

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The porphyrias are a group of inherited metabolic disorders of heme biosynthesis which result from a partial deficiency in one of its seven specific enzymes, after its first and rate limiting enzyme, delta-aminolevulinic acid synthetase. They can be classified on the basis of their clinical manifest...

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Detalles Bibliográficos
Autores principales:	Parera, V.E., De Siervi, A., Varela, L., Rossetti, M.V., Batlle, A.M.
Formato:	Artículo publishedVersion
Publicado:	2003
Materias:	acute intermittent porphyria Argentina genetics hepatic porphyria human metabolism mutation review Humans Mutation Porphyria, Acute Intermittent Porphyrias, Hepatic
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_01455680_v49_n4_p493_Parera https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_01455680_v49_n4_p493_Parera_oai
Aporte de:	Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires

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