Cytochrome P4501A1 polymorphisms in a Caucasian population with porphyria cutanea tarda
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Reference32 articles.
1. Decreased Activity of Hepatic Uroporphyrinogen Decarboxylase in Sporadic Porphyria Cutanea Tarda
2. Identification of Two Types of Porphyria Cutanea Tarda by Measurement of Erythrocyte Uroporphyrinogen Decarboxylase
3. Familial and sporadic porphyria cutanea
4. Uroporphyrinogen Decarboxylase Structural Mutant (Gly281→Glu) in a Case of Porphyria
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1. Acute intermittent porphyria: a disease with low penetrance and high heterogeneity;Frontiers in Genetics;2024-08-12
2. High penetrance of acute intermittent porphyria in a Spanish founder mutation population and CYP2D6 genotype as a susceptibility factor;Orphanet Journal of Rare Diseases;2019-02-26
3. ASSOCIATION OF ALLELIC VARIANTS OF GENES OF DETOXIFICATION SYSTEM WITH CLINICAL PRESENTATION OF ACUTE INTERMITTENT PORPHYRIA;GEMATOL TRANSFUZIOL;2016
4. Cutaneous porphyrias part I: epidemiology, pathogenesis, presentation, diagnosis, and histopathology;International Journal of Dermatology;2013-11-21
5. CYP1A2*1F and GSTM1 Alleles Are Associated with Susceptibility to Porphyria Cutanea Tarda;Molecular Medicine;2010-10-15
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