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
The molecular genetic analysis of the expanding pachyonychia congenita case collection.
Wilson NJ et al.
The British Journal of Dermatology, 2014
Novel mutation (p.L91P, c.272T>C) of keratin 17 in a case with pachyonychia congenita type 2.
Ichimiya M et al.
The Journal of Dermatology, 2013
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