A novel mutation of the keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-4632.2009.04295.x/fullpdf
Reference6 articles.
1. Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21;Reis;Hum Genet,1992
2. Identification of the keratin 9 (KRT9) N161S mutation in a Chinese kindred with epidermolytic palmoplantar keratoderma;Wenhua;Eur J Dermatol,2008
3. Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma;Hennies;Hum Genet,1994
4. Keratin 9 gene mutations in five Korean families with epidermolytic palmoplantar keratoderma;Lee;Exp Dermatol,2003
5. Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motif;Coleman;Br J Dermatol,1999
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1. Identification of a Novel KRT9 Frameshift Mutation in a Chinese Pedigree with Epidermolytic Palmoplantar Keratoderma;INTERNATIONAL JOURNAL OF HUMAN GENETICS;2021-11-25
2. Keratin 9L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review;Molecular Genetics & Genomic Medicine;2019-09-16
3. Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma;Frontiers in Genetics;2019-01-07
4. Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma;Cellular Physiology and Biochemistry;2018
5. Mutations in the highly conserved 1A rod domain of keratin 9 responsible for epidermolytic palmoplantar keratoderma in four Chinese families;The Journal of Dermatology;2017-10-17
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