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: Contribution to journalLetterpeer-review

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

All Science Journal Classification (ASJC) codes

  • Dermatology

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