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EJHG.2012.146
EJHG.2012.146
http://dx.doi.org/10.1038/EJHG.2012.146
A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease
P356
Q24632463-D9BBBD60-839D-4AC6-AC32-49D5262F21B3
P356
EJHG.2012.146
http://dx.doi.org/10.1038/EJHG.2012.146