P5.45 Recurrent rhabdomyolysis caused by LPIN 1 gene mutation in a patient affected by Charcot–Marie–Tooth 1A
A. Nascimento, C. Ortez, C. Jimenez-Mallabrera, J. Garcia-Villoria, E. Blazquez, C. Jou, J. Corbera, A. Garcia, J. ColomerVolume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.1074
File:
PDF, 61 KB
english, 2011