A molecular, enzymatic and clinical study in a family with hereditary coproporphyria
Author:
Affiliation:
1. ; Division of Clinical Biochemistry; Philipps University Hospital; Marburg Germany
2. ; Centre Français des Porphyries, INSERM U409; Hôpital Louis Mourier; Colombes France
3. Division of Clinical Biochemistry; Postfach 12 20 Marburg 35002 Germany
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1016598207397/fullpdf
Reference13 articles.
1. B. Porphyrins and Porphyrin Precursors
2. Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase;Doss;Int J Biochem,1978
3. Heredit Pre Koproporphyrie in der Bundesrepublik Deutschland;Doss;J Clin Chem Clin Biochem,1978
4. ‘Glucose effect’ and rate limiting function of uroporphyrinogen synthase on porphyrin metabolism in hepatocyte culture: relationship with human acute hepatic porphyrias;Doss;J Clin Chem Clin Biochem,1985
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