Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase-Reference-Cited by-同舟云学术

Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase

Published:1978-01 Issue:12 Volume:9 Page:911-916
ISSN:0020-711X
Container-title:International Journal of Biochemistry
language:en
Short-container-title:International Journal of Biochemistry

Author:

Doss M.

Publisher

Elsevier BV

Subject

Biochemistry

Reference11 articles.

1. Reduced ferrochelatase activity: a defect common to porphyria variegata and protoporphyria;Becker;Br. J. Haemat.,1977

2. Metabolism of δ-aminolevulinic acid and porphobilinogen in human erythrocytes in acute intermittent porphyria;Doss,1974

3. Urinary porphyrin excretion pattern and isomer distribution of I and III in human porphyrin disorders;Doss,1976

4. Uroporphyrinogen-Synthase in Erythrozyten bei akuter intermittierender Porphyrie (AI P): Neue pathobiochemische Aspekte;Doss;J. Clin. Chem. Clin. Biochem.,1978

5. Biochemical and clinical relationships among the hereditary acute hepatic porphyrias;Doss;Abstracts of the International Symposium on Porphyrias and Lead Intoxication: J. Clin. Chem. Clin. Biochem.,1978

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