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

This study was supported in part by Ricerca Corrente 2012?2015 from the Italian Ministry of Health.

Autori: Gagliardi S, Ricca I, Ferrarini A, Valente M, Grieco GS, Piccolo G, Alfonsi E, Delledonne M, Cereda C. Br J.
Dermatol. 2017 Jul;177(1):284-286. Epub 2017 Jun 14.

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