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TRPV4 mutation causing dominantly inherited scapuloperoneal spinal muscle atrophy
Sanaker, P., Bindoff, L.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.144
Date:
October, 2015
File:
PDF, 208 KB
english, 2015