Acute Intermittent Porphyria in a Man with Dual Enzyme Deficiencies
Author:
Affiliation:
1. Centro de Investigaciones sobre Porfirinas y Porfirias (CIPYP)-CONICET, Hospital de Clínicas-UBA, Buenos Aires, Argentina
2. Hospital General de Agudos, Buenos Aires, Argentina
Abstract
Funder
UBA
Publisher
Hindawi Limited
Subject
General Medicine
Link
http://downloads.hindawi.com/journals/crig/2020/8873219.pdf
Reference25 articles.
1. Hepta- and hexa-carboxylic porphyrinogen intermediates in haem biosynthesis;A. H. Jackson;Annals of Clinical Research,1976
2. Porphyrias
3. Familial and sporadic porphyria cutanea
4. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects
5. Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: Evidence for an ancestral founder of the common G111R mutation
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