Associated Papers
Identification of a KRT9 gene variant and preimplantation genetic diagnosis in a Chinese family with KRT9-palmoplantar epidermal differentiation disorder.
Lin D et al.
Hereditas, 2025
Keratin 9 L164P mutation in a Chinese pedigree with epidermolytic palmoplantar keratoderma, cytokeratin analysis, and literature review.
Liu X et al.
Molecular Genetics & Genomic Medicine, 2019
Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma.
Xiao H et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology, 2018
Genetic Analysis of KRT9 Gene Revealed Previously Known Mutations and Genotype-Phenotype Correlations in Epidermolytic Palmoplantar Keratoderma.
Li Y et al.
Frontiers in Genetics, 2018
A recurrent p.M157R mutation of keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma and literature review.
Liang YH et al.
International Journal of Dermatology, 2014
The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigrees.
Liu WT et al.
Anatomical Record (hoboken, N.j. : 2007), 2012
Mutations in the keratin 9 gene in Pakistani families with epidermolytic palmoplantar keratoderma.
Shimomura Y et al.
Clinical and Experimental Dermatology, 2010
Mutation M157R of keratin 9 in a Chinese family with epidermolytic palmoplantar keratoderma.
Zhao JJ et al.
International Journal of Dermatology, 2008
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