Palmoplantar keratoderma and Charcot–Marie–Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole-exome sequencing

S. Gagliardi, I. Ricca, A. Ferrarini, M. Valente, G. S. Grieco, G. Piccolo, E. Alfonsi, M. Delledonne, C. Cereda

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)284-286
Number of pages3
JournalBritish Journal of Dermatology
Volume177
Issue number1
DOIs
Publication statusPublished - Jul 1 2017

ASJC Scopus subject areas

  • Dermatology

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