Pachyonychia congenita: pathogenesis of pain and approaches to treatment
Author:
Affiliation:
1. Centre for Cell Biology and Cutaneous Research, Blizard Institute, The Faculty of Medicine and Dentistry, Queen Mary University of London , London , UK
2. Department of Dermatology, Royal London Hospital, Barts Health NHS Trust , London , UK
Abstract
Funder
LEO Foundation
Publisher
Oxford University Press (OUP)
Link
https://academic.oup.com/ced/advance-article-pdf/doi/10.1093/ced/llae199/58933842/llae199.pdf
Reference74 articles.
1. A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita;Eliason;J Am Acad Dermatol,2012
2. Keratin 16 and keratin 17 mutations cause pachyonychia congenita;McLean;Nat Genet,1995
3. Mutation of a type II keratin gene (K6a) in pachyonychia congenita;Bowden;Nat Genet,1995
4. A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2;Smith;Hum Mol Genet
5. A large mutational study in pachyonychia congenita;Wilson;J Invest Dermatol,2011
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