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 sequenc.

Autor: Gagliardi, S., Ricca, I., Ferrarini, A., Valente, M., Grieco, G.S., Piccolo, G., Alfonsi, E., Delledonne, M., Cereda, C.
Zdroj: British Journal of Dermatology; Jul2017, Vol. 177 Issue 1, p284-286, 3p, 1 Color Photograph, 1 Diagram
Databáze: Complementary Index
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