Art

J-GLOBAL ID：201902250138436588   Reference number：19A0419279

The first Japanese case of familial porphyria cutanea tarda diagnosed by a UROD mutation

UROD変異により診断された家族性晩発性皮膚ポルフィリン症の初の日本人症例

Author (6)： Matsui Akinobu (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan) ,  Akasaka Eijiro (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan) ,  Rokunohe Daiki (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan) ,  Matsuzaki Yasushi (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan) ,  Sawamura Daisuke (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan) ,  Nakano Hajime (Department of Dermatology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan)
Material： Journal of Dermatological Science  (J Dermatol Sci)
Volume： 93  Issue： 1  Page： 65-67  Publication year： Jan. 2019 
JST Material Number： W1280A  ISSN： 0923-1811  Document type： Article
Article type： 短報  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： *porphyria ,...
Semi thesaurus term： *家族性晩発性皮膚ポルフィリン症 ,...

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JST classification (2)： Dermatlogic diagnosis  (GF02000J) ,  Diagnostics of congenital diseases, deformities.  (GD03020G)

Terms in the title (6)： 変異 ,  診断 ,  家族 ,  晩発性皮膚ポルフィリン症 ,  日本人 ,  症例