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s12017-014-8307-9
s12017-014-8307-9
https://scigraph.springernature.com/pub.10.1007/s12017-014-8307-9
Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease.
P2888
Q45107853-A4A19B50-D577-4E50-A352-92481F7DAA33
P2888
s12017-014-8307-9
https://scigraph.springernature.com/pub.10.1007/s12017-014-8307-9