Associated Papers
Mutation analysis of the KRT17 gene in steatocystoma multiplex and a brief literature review.
Zhang B et al.
Clinical and Experimental Dermatology, 2020
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
The molecular genetic analysis of the expanding pachyonychia congenita case collection.
Wilson NJ et al.
The British Journal of Dermatology, 2014
A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb.
Tsuda T et al.
The British Journal of Dermatology, 2008
Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.
Agarwala M et al.
Indian Journal of Dermatology, 0
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