Uroporphyrinogen Decarboxylase Structural Mutant (Gly281→Glu) in a Case of Porphyria
Author:
Affiliation:
1. aculty of Medicine X. Bichat, Department of Biochemistry, Hospital Louis Mourier, Colombes, France.
2. Institut National de la Santé et de la Recherche Médicale, U. 160, Hospital Beaujon, Clichy, France.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference15 articles.
1. DEVERNEUIL, H, ENZYMATIC AND IMMUNOLOGICAL STUDIES OF UROPORPHYRINOGEN DECARBOXYLASE IN FAMILIAL PORPHYRIA CUTANEA-TARDA AND HEPATOERYTHROPOIETIC PORPHYRIA, AMERICAN JOURNAL OF HUMAN GENETICS 36: 613 (1984).
2. DEVERNEUIL, H, MOLECULAR ANALYSIS OF UROPORPHYRINOGEN DECARBOXYLASE DEFICIENCY IN A FAMILY WITH 2 CASES OF HEPATOERYTHROPOIETIC PORPHYRIA, JOURNAL OF CLINICAL INVESTIGATION 77: 431 (1986).
3. ELDER, G.H., HEPATOERYTHROPOIETIC PORPHYRIA - A NEW UROPORPHYRINOGEN DECARBOXYLASE DEFECT OR HOMOZYGOUS PORPHYRIA CUTANEA-TARDA, LANCET 1: 916 (1981).
4. A simple and very efficient method for generating cDNA libraries
5. KAPPAS, A, METABOLIC BASIS INHE: 1301 (1983).
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