ID 429 – Clinical and electrophysiological follow-up study of a patient with congenital myasthenic syndrome (CMS) associated with mutations in the gen of the agrin ( AGRN )
Fernandez, J.M, Mederer, S, Diéguez-Varela, C, Padrón, M.L, Navarro, C, Maselli, R
Published in Clinical neurophysiology (01.03.2016)
Published in Clinical neurophysiology (01.03.2016)
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Journal Article
P1030: Clinical and electrophysiological follow-up study of a patient with congenital myasthenic syndrome (CMS) associated with mutations in the gene of the agrin ( AGRN )
Fernandez, J.M, Mederer-Hengstl, S, Diéguez-Varela, C, Padron, M.L, Navarro, C, Maselli, R.L
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Journal Article