THE PRIMARY ENZYME DEFECT IN HEREDITARY COPROPORPHYRIA

The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1988 · 7.8K citations

Life Sciences, Genetics, Molecular Genetics +13

THE OCCURRENCE AND DETERMINATION OF δ-AMINOLEVULINIC ACID AND PORPHOBILINOGEN IN URINE

D. Mauzerall, S. Granick · Journal of Biological Chemistry · 1956 · 1.6K citations · Full text

Pharmacy, Biochemistry, Toxicology +3

Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.

Herbert L. Bonkowsky, Joseph R. Bloomer, Paul S. Ebert et al. · Journal of Clinical Investigation · 1975 · 250 citations · Full text

Life Sciences, Biochemistry, Cell Biology +11

Heme Biosynthesis in Intermittent Acute Porphyria: Decreased Hepatic Conversion of Porphobilinogen to Porphyrins and Increased Delta Aminolevulinic Acid Synthetase Activity

Lars Strand, Bertram F. Felsher, Allan G. Redeker et al. · Proceedings of the National Academy of Sciences · 1970 · 173 citations · Full text

Life Sciences, Biochemistry, Genetics +16

Decreased Red Cell Uroporphyrinogen I Synthetase Activity in Intermittent Acute Porphyria

Lars Strand, Urs Meyer, Bertram F. Felsher et al. · Journal of Clinical Investigation · 1972 · 130 citations · Full text

Life Sciences, Biochemistry, Genetics +8