Familial and sporadic porphyria cutanea

Author:

de Verneuil H.,Aitken G.,Nordmann Y.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. Blekkenhorst, G., Pimstone, N. R., Eales, L.: Porphyria cutanea tarda in South Africa: The metabolic basis of discorded haem biosynthesis. In: Porphyrins in Human Diseases, Proc. Int. Porphyrin Meet. 1st, Freiburg, (M. Doss, ed.), pp. 299?311. Basel: S, Karger 1976

2. Blincoe, C.: The simultaneous separation and washing of erythrocytes. Clin. Chim. Acta 57, 297?300 (1974)

3. Edmondson, P. R., Schwartz, S.: Studies of the uroporphyrins. III. An improved method for the decarboxylation of uroporphyrin. J. Biol. Chem. 205, 605?609 (1953)

4. Elder, G. H.: Identification of a group of tetracarboxylate porphyrins, containing one acetate and three propionate ?-substituents, in faeces from patients with symptomatic cutaneous hepatic porphyria and from rats with porphyria due to hexachlorobenzene. Biochem. J. 126, 877?891 (1972)

5. Elder, G. H.: Porphyrin metabolism in porphyria cutanea tarda. Semin. Hematol. 14, 227?242 (1975)

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