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Article

A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene.

The British journal of dermatology - 1 Feb 2013

Fonseca D J, Rojas R F, Vergara J I, Ríos X, Uribe C, Chávez L, Velandia F, Vargas C I, Restrepo C M, Laissue P

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Identifiers

PMID: 22834809
DOI: 10.1111/j.1365-2133.2012.11181.x

Genes

KRT1

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