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A Finnish mutation in SCN4A gene causes predominantly myalgic phenotype
Palmio, J., Sandell, S., Penttilä, S., Udd, B.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.093
Date:
October, 2015
File:
PDF, 207 KB
english, 2015