HLA-A3 and -B7 in porphyria cutanea tarda
Author:
Publisher
Wiley
Subject
Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0039.1984.tb00402.x/fullpdf
Reference14 articles.
1. Iron-overload associated myopathy in patients on maintenance hemodialysis: a histocompatibility linked disorder;Bregman;Lancet,1980
2. Analytical and preparative thin layer chromotography of porphyrinmethylesters;Doss;Klin Chem Klin Biochem,1970
3. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda;Elder;N Engl J Med,1978
4. Red cell uroporphyrinogen decarboxylase in porphyria;Felsher;N Engl J Med,1978
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1. Porphyria cutanea tarda;Der Hautarzt;2016-01-07
2. Porphyria Cutanea Tarda and Related Disorders;The Porphyrin Handbook;2003
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4. C282Y and H63D mutations in the HFE gene are not associated with porphyria cutanea tarda in bulgaria;Hepatology;1999-12
5. Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload;Hepatology;1998-01
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