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Graziola, F. et al. (n.d.). Intrafamilial heterogeneity of clinical phenotype of PRRT2 mutations. European journal of paediatric neurology. pp. e217-. [Online].
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Graziola, F. et al. (n.d.). Intrafamilial heterogeneity of clinical phenotype of PRRT2 mutations. European journal of paediatric neurology. pp. e217-. [Online].