P5.20 Limb Girdle Congenital Myasthenia Syndrome associated with mutations in GFPT1 gene. Report of two patients

✍ Scribed by J. Colomer; A. Nascimento; C. Ortez; C. Jimenez-Mallabrera; C. Jou; J. Corbera; V. Guergueltcheva; J. Senderek; J.S. Müller; H. Lochmüller

• Book ID: 116794862
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 59 KB
• Volume: 21
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2011.06.1049