The second Japanese case of porphyria cutanea tarda with a novel genetic mutation in UROD
Author:
Affiliation:
1. Division of Dermatology Nippon Medical School Musashikosugi Hospital Kawasaki Japan
2. Department of Dermatology Hirosaki University Graduate School of Medicine Hirosaki Japan
3. Department of Dermatology Nippon Medical School Tokyo Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16156
Reference7 articles.
1. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects
2. A case of porphyria cutanea tarda;Nishiura T;Dermatol Chronicle,1960
3. The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation
4. Porphyrias in Japan: compilation of all cases reported through 2010;Kondo M;ALA Porphyrin Sci,2012
5. Erythrocyte uroporphyrinogen decarboxylase activity in 80 unrelated patients with porphyria cutanea tarda
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