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Article

Morphological and genetic analysis of steatocystoma multiplex in an Asian family with pachyonychia congenita type 2 harbouring a KRT17 missense mutation.

The British journal of dermatology - 1 Feb 2009

Kanda M, Natsuga K, Nishie W, Akiyama M, Nagasaki A, Shimizu T, Shimizu H

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Identifiers

PMID: 19120334
DOI: 10.1111/j.1365-2133.2008.08983.x

Genes

KRT17

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