Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference34 articles.
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2. Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda?;Elder;Lancet,1981
3. Immunoreactive uroporphyrinogen decarboxylase in the liver in porphyria cutanea tarda;Elder;Lancet,1985
4. An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity;Kushner;J Clin Invest,1976
5. Familial and sporadic porphyria cutanea: two different diseases;de Verneuil;Hum Genet,1978
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