Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations von Schara, Ulrike, Christen, Hans-Jürgen, Durmus, Hacer, Hietala, Marja, Krabetz, Kerstin, Rodolico, Carmelo, Schreiber, Gudrun, Topaloglu, Haluk, Talim, Beril, Voss, Wolfgang, Pihko, Helena, Abicht, Angela, Müller, Juliane S, Lochmüller, Hanns

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