The P25L mutation in the KRT5 gene in a Japanese family with epidermolysis bullosa simplex with mottled pigmentation
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2004.05820.x/fullpdf
Reference9 articles.
1. Epidermolysis bullosa simplex with mottled pigmentation
2. Epidermolysis bullosa simplex with Mottled Pigmentation
3. Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation
4. The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.
5. A Mutation in the V1 Domain of Keratin 5 Causes Epidermolysis Bullosa Simplex with Mottled Pigmentation
Cited by 13 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. Novel variants in LAMA3 and COL7A1 and recurrent variant in KRT5 underlying epidermolysis bullosa in five Chinese families;Frontiers of Medicine;2022-03-21
2. Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT 5;The Journal of Dermatology;2019-01-28
3. Epidermolysis Bullosa Simplex with Mottled Pigmentation: A Family Report and Review;Pediatric Dermatology;2012-05-29
4. Epidermolysis bullosa simplex with mottled pigmentation - mutation analysis proved the diagnosis in a four-generation pedigree;EUR J DERMATOL;2010
5. A transient epidermolysis bullosa simplex-like phenotype associated with bexarotene treatment in a G138E KRT5 heterozygote;Journal of Cutaneous Pathology;2010-05-17
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