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Mori, C. et al. (n.d.). A family with both X‐linked dominant Charcot–Marie–Tooth disease and myotonic dystrophy type 1 mutations with phenotypic variations. Neurology and clinical neuroscience. 7 (2), pp. 88-90. [Online].
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Mori, C. et al. (n.d.). A family with both X‐linked dominant Charcot–Marie–Tooth disease and myotonic dystrophy type 1 mutations with phenotypic variations. Neurology and clinical neuroscience. 7 (2), pp. 88-90. [Online].