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SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype
Bugiardini, E., Rivolta, I., Binda, A., Soriano Caminero, A., Cirillo, F., Cinti, A., Giovannoni, R., Botta, A., Cardani, R., Wicklund, M.P., Meola, G.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.01.006
Date:
April, 2015
File:
PDF, 1.48 MB
english, 2015