P5.45 Recurrent rhabdomyolysis caused by LPIN 1 gene mutation in a patient affected by Charcot–Marie–Tooth 1A

✍ Scribed by A. Nascimento; C. Ortez; C. Jimenez-Mallabrera; J. Garcia-Villoria; E. Blazquez; C. Jou; J. Corbera; A. Garcia; J. Colomer

• Book ID: 116794887
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 61 KB
• Volume: 21
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2011.06.1074