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
Author Information: Genomic and Post‐Genomic Center
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