THE PRIMARY ENZYME DEFECT IN HEREDITARY COPROPORPHYRIA
- 1 December 1976
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 308 (7997) , 1217-1219
- https://doi.org/10.1016/s0140-6736(76)91143-0
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- THE OCCURRENCE AND DETERMINATION OF δ-AMINOLEVULINIC ACID AND PORPHOBILINOGEN IN URINEPublished by Elsevier ,2021
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- The measurement of the synthetic rate of bilirubin from hepatic hemes in patients with acute intermittent porphyriaJournal of Clinical Investigation, 1971
- HEPATIC δ-AMINOLÆVULINIC ACID SYNTHETASE IN AN ATTACK OF HEREDITARY COPROPORPHYRIA AND DURING REMISSIONThe Lancet, 1971
- Heme Biosynthesis in Intermittent Acute Porphyria: Decreased Hepatic Conversion of Porphobilinogen to Porphyrins and Increased Delta Aminolevulinic Acid Synthetase ActivityProceedings of the National Academy of Sciences, 1970
- Biochemical Defects in Two Types of Human Hepatic PorphyriaNew England Journal of Medicine, 1970
- Hereditary CoproporphyriaAnnals of Internal Medicine, 1968
- HEREDITARY COPROPORPHYRIAThe Lancet, 1967