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A third case of congenital myasthenic syndrome caused by mutations in SCN4A
Witting, N., Werlauff, U., Ballegaard, M., Vissing, J.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.091
Date:
October, 2015
File:
PDF, 207 KB
english, 2015