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G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations

✍ Scribed by U. Schara; H. Christen; M. Hietala; Z. Hoovey; K. Krabetz; C. Rodolico; G. Schreiber; H. Topaloglu; W. Voss; A. Abicht; J. Müller; H. Lochmüller


Book ID
116793041
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
49 KB
Volume
17
Category
Article
ISSN
0960-8966

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