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

: Schara U, Christen H J, Durmus H, Hietala M, Krabetz K, Rodolico C, Schreiber G, Topaloglu H, Talim B, Voss W, Pihko H, Abicht A, Müller J S, Lochmüller H

: 2010

: European Journal of Paediatric Neurology

: 4

: 14

: 4

: 326

: 333

: 8

: 1090-3798

DOI: https://doi.org/10.1016/j.ejpn.2009.09.009