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June 15, 1972New England Journal of Medicine

Intermittent Acute Porphyria — Demonstration of a Genetic Defect in Porphobilinogen Metabolism

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Authors

UMUrs MeyerLSLars StrandMDM. Doss

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Meyer et al. (1972) studied this question.

synapsesocial.com/papers/6a8bdc42c716e89f35deff71https://doi.org/10.1056/nejm197206152862401
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Steroid Induction of Porphyrin Synthesis in Liver Cell Culture1968 · 145 citations
  2. 2A SUGGESTED CONTROL GENE MECHANISM FOR THE EXCESSIVE PRODUCTION OF TYPES I AND III PORPHYRINS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA1964 · 55 citations
  3. 3Heme Biosynthesis in Intermittent Acute Porphyria: Decreased Hepatic Conversion of Porphobilinogen to Porphyrins and Increased Delta Aminolevulinic Acid Synthetase Activity1970 · 173 citations