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Medline ® Abstract for Reference 48

of 'Overview and classification of the inherited ichthyoses'

48
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A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene.
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Fonseca DJ, Rojas RF, Vergara JI, Ríos X, Uribe C, Chávez L, Velandia F, Vargas CI, Restrepo CM, Laissue P
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Br J Dermatol. 2013 Feb;168(2):456-8.
 
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PMID