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A novel form of CAP myopathy in absence of heart disease associated with recessive TTN gene mutations
Jou, C., Ortez, C., Jimenez-Mallebrera, C., Romero, N., Bouchier, G., Fernández-Marmiesse, A., Couce, M., Carrascosa-Romero, M., Blancas, A., Ribalta, T., Colomer, J., Nascimento, A.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.362
Date:
October, 2015
File:
PDF, 213 KB
english, 2015