Genetic Blistering Diseases
Author:
Publisher
Wiley-Blackwell
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/9781444317633.ch39/fullpdf
Reference475 articles.
1. Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation;Hovnanian;Am J Hum Genet,1997
2. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease;Hu;Nat Genet,2000
3. Hereditare anlage zur blasenbildung (epidermolysis bullosa hereditare);Koebner;Dtsch Med Wochenschr,1886
Cited by 4 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. Successful Management of Epidermolysis Bullosa Pruriginosa with Oral Thalidomide: A Case Report of Rare Dystrophic EB Subset;Indian Journal of Dermatology;2024-09-13
2. How to Take a Skin Biopsy Correctly to Diagnose Epidermolysis Bullosa and Autoimmune Bullous Diseases;Blistering Diseases;2015
3. Acantholysis revisited: Back to basics;Indian Journal of Dermatology, Venereology, and Leprology;2013
4. Immunofluorescence antigen mapping for hereditary epidermolysis bullosa;Indian Journal of Dermatology, Venereology, and Leprology;2012
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