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A case of CMT 1 B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemiaLUIGETTI, M; MODONI, A; POMPONI, M. G et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2010, Vol 112, Num 9, pp 794-797, issn 0303-8467, 4 p.Article