A novel keratin 9 gene mutation (Asn160His) in a Taiwanese family with epidermolytic palmoplantar keratoderma
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2004.01497.x/fullpdf
Reference9 articles.
1. Zur Kenntniss des Keratoma hereditarium palmare et plantare
2. Ultrastructural Changes Resulting from Keratin-9 Gene Mutations in Two Families with Epidermolytic Palmoplantar Keratoderma
3. Genes for intermediate filament proteins and the draft sequence of the human genome
4. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation
5. Cytokeratin No. 9, an epidermal type I keratin characteristic of a special program of keratinocyte differentiation displaying body site specificity.
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1. Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma;Frontiers in Genetics;2019-01-07
2. A recurrent p.M157R mutation of keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma and literature review;International Journal of Dermatology;2014-06-05
3. The Most Common Mutation of KRT9, c.C487T (p.R163W), in Epidermolytic Palmoplantar Keratoderma in Two Large Chinese Pedigrees;The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology;2012-01-20
4. 9 Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010
5. Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010
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