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

✍ Scribed by Ulrike Schara; Hans-Jürgen Christen; Hacer Durmus; Marja Hietala; Kerstin Krabetz; Carmelo Rodolico; Gudrun Schreiber; Haluk Topaloglu; Beril Talim; Wolfgang Voss; Helena Pihko; Angela Abicht; Juliane S. Müller; Hanns Lochmüller

Book ID: 113590486
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 521 KB
Volume: 14
Category: Article
ISSN: 1090-3798
DOI: 10.1016/j.ejpn.2009.09.009

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