Myotonia permanens with neonatal onset associated with a p.Gly1306Glu mutation in the SCN4A gene.

Myotonia permanens with neonatal onset associated with a p.Gly1306Glu mutation in the SCN4A gene / V. Sansone, S. Pagliarani, S. Lucchiari, A. Zanolini, B. Fossati, M.C. Panzeri, G.P. Comi, G. Meola. ((Intervento presentato al convegno 19th Meeting of the European Neurological Society tenutosi a null nel null.