Associated Papers
Mutational analysis of epidermal and hyperproliferative type I keratins in mild and moderate psoriasis vulgaris patients: a possible role in the pathogenesis of psoriasis along with disease severity.
Elango T et al.
Human Genomics, 2018
29784039 (PubMed )
Supplement: 40246_2018_158_MOESM2_ESM.xlsx › K17
Steatocystoma multiplex is associated with the R94C mutation in the KRTl7 gene.
Liu Q et al.
Molecular Medicine Reports, 2015
A novel missense mutation of keratin 17 gene in a chinese family with steatocystoma multiplex.
Ha WW et al.
Annals of Dermatology, 2013
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