O.21 Congenital Myasthenic Syndrome (CMS), autophagic myopathy, and cognitive dysfunction caused by mutations in DPAGT1

✍ Scribed by Selcen, D.; Shen, X.M.; Li, Y.; Wieben, E.D.; Engel, A.G.

• Book ID: 122521111
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 48 KB
• Volume: 23
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2013.06.731