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

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

Research output: Articles / NotesLetterpeer-review

10 Scopus citations
Original languageEnglish
Pages (from-to)456-458
Number of pages3
JournalBritish Journal of Dermatology
Issue number2
StatePublished - Feb 2013

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