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Dive into the research topics of 'Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK'. Together they form a unique fingerprint.- Sort by
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Lorenzo Maggi, R. Brugnoni, V. Scaioli, T. L. Winden, L. Morandi, A. G. Engel, R. Mantegazza, P. Bernasconi
Research output: Contribution to journal › Letter › peer-review