Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutations

Autor: Natera-de Benito, D. *, Bestué, M., Vilchez, J.J., Evangelista, T., Töpf, A., García-Ribes, A., Trujillo-Tiebas, M.J., García-Hoyos, M., Ortez, C., Camacho, A., Jiménez, E., Dusl, M., Abicht, A., Lochmüller, H., Colomer, J., Nascimento, A.
Zdroj: In Neuromuscular Disorders February 2016 26(2):153-159
Databáze: ScienceDirect