The 6-year follow-up of a Japanese patient with silent erythropoietic protoporphyria
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference10 articles.
1. The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH;Gouya;Nat Genet,2002
2. Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestation;Gouya;Blood,1999
3. Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria;Gouya;Am J Hum Genet,2006
4. Novel ferrochelatase mutations in Japanese patients with erythropoietic protoporphyria: high frequency of the splice site modulator IVS3-48C polymorphism in the Japanese population;Nakano;J Invest Dermatol,2006
5. The cases of erythropoietic protoporphyria diagnosed by genetic analysis of the ferrochelatase gene;Furuichi;Rinsho Derma,2011
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dentigerous cyst excision using shading films in a patient with erythropoietic protoporphyria;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2022-07
2. Inherited genetic late‐onset erythropoietic protoporphyria: A systematic review of the literature;Photodermatology, Photoimmunology & Photomedicine;2021-02-21
3. Erythropoietic Protoporphyria in a Japanese Population;Acta Dermato Venereologica;2019
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