arginine has been researched along with Epidermolytic Palmoplantar Keratoderma Vorner Type in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, XL; Du, ZF; Ke, HP; Liu, WT; Lu, JJ; Yu, D; Zhang, XN; Zhao, Y | 1 |
Chiu, HC; Chu, CY; Jee, SH; Liaw, SH; Lin, PJ; Sheen, YS | 1 |
2 other study(ies) available for arginine and Epidermolytic Palmoplantar Keratoderma Vorner Type
Article | Year |
---|---|
The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigrees.
Topics: Adult; Arginine; Asian People; Female; Foot; Genes, Dominant; Hand; Humans; Keratin-9; Keratoderma, Palmoplantar, Epidermolytic; Male; Mutation; Pedigree; Protein Structure, Secondary; Protein Structure, Tertiary | 2012 |
Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads.
Topics: Arginine; Female; Hand Deformities; Humans; Keratin-9; Keratoderma, Palmoplantar, Epidermolytic; Male; Mutation; Pedigree; Tryptophan | 2007 |