Novel<i> GDAP1</i> Mutation in a Vietnamese Family with Charcot-Marie-Tooth Disease

Abstract

Our study expands the mutational spectrum of <i>GDAP1</i>-related CMT disease with the new and unreported <i>GDAP1</i> variant. Alterations in <i>GDAP1</i> gene should be evaluated as CMT causing variants in the Vietnamese population, predominantly axonal form of neuropathy in CMT disease.