AKRT1gene mutation related to epidermolytic ichthyosis in a Chinese family
Author:
Affiliation:
1. Department of Dermatology; Second Hospital of Ji Lin University; Changchun China
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12649/fullpdf
Reference8 articles.
1. Mutation in the rod domains of keratin 1 and 10 in epidermolytic hyperkeratosis;Rothnagel;Science,1992
2. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009;Oji;J Am Acad Dermatol,2010
3. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event;Lacz;Int J Dermatol,2005
4. Bullous ichthyosiform erythroderma in a child born to a parent with systematized linear epidermolytic hyperkeratosis;Akhyani;Int J Dermatol,2009
5. Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation;Morais;Eur J Dermatol,2009
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