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S12017-014-8307-9
S12017-014-8307-9
http://dx.doi.org/10.1007/S12017-014-8307-9
Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease.
P356
Q45107853-03FFDDE7-CE2D-4FAE-AA2F-E29D629B98CB
P356
S12017-014-8307-9
http://dx.doi.org/10.1007/S12017-014-8307-9