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Marrosu MG, Vaccaugiu S, Marrosu G, Vannelli A, Cianchetti C, Muntoni F. Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene. Neurol 50: 1397-1401, 1998.","DOI":"10.1212\/WNL.50.5.1397"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Mastaglia FL, Nowak KJ, Stell R, et al. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 67: 174-179, 1999.","DOI":"10.1136\/jnnp.67.2.174"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Shy ME, Jáni A, Krajewski K, et al. Phenotypic clustering in MPZ mutations. Brain 127: 371-384, 2004.","DOI":"10.1093\/brain\/awh048"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. De Jonghe P, Timmerman V, Ceuterick C, et al. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype. 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