Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin-related proteins(PMP22, MPZ and Cx32): a clinicopathologi
DemyelinatingandaxonalfeaturesofCharcot–Marie–Toothdiseasewithmutationsofmyelin-relatedproteins(PMP22,MPZandCx32):aclinicopathologicalstudyof205Japanesepatients,Keywords,Abbreviations,PatientsandDNAdiagnosis,Clinicalassessment,Electrophysiologicalanalysis,Pa
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