The role of inherited and acquired factors in the development of porphyria cutanea tarda in the Argentinean population

Author:

Méndez Manuel,Rossetti María V.,Del C. Batlle Alcira M.,Parera Victoria E.

Publisher

Elsevier BV

Subject

Dermatology

Reference54 articles.

1. Disorders of heme biosynthesis: X-linked sideroblastic anemia and the porphyrias;Anderson,2000

2. Hepta and hexa-carboxylic porphyrinogen intermediates in haem biosynthesis;Jackson;Ann Clin Res,1976

3. Familial and sporadic porphyria cutanea: two different diseases;De Verneuil;Hum Genet,1978

4. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda;Elder;N Engl J Med,1978

5. Analysis of uroporphyrinogen decarboxylase complementary DNAs in sporadic porphyria cutanea tarda;Garey;Gastroenterology,1993

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