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. - In: BRITISH JOURNAL OF DERMATOLOGY. - ISSN 0007-0963. - 177:1(2017 Jul), pp. 284-286. [10.1111/bjd.15066]
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
C. CeredaUltimo
2017
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