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P.1.10 siRNA-mediated allele-specific silencing of a dominant negative COL6A3 mutation causing Ullrich Congenital muscular dystrophy
Bolduc, V., Zou, Y., Bonnemann, C.G.Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.394
Date:
October, 2013
File:
PDF, 46 KB
english, 2013