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Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations inMUSK

✍ Scribed by Maggi, Lorenzo; Brugnoni, R.; Scaioli, V.; Winden, T. L.; Morandi, L.; Engel, A. G.; Mantegazza, R.; Bernasconi, P.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

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Clinical variability of CMS-EA (congenit

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Phenotype genotype analysis in 15 patien

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Ephedrine therapy in eight patients with

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Long-term follow-up in patients with con

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G.P.10.01 Long-term follow-up in patient

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