Abstract
Erratum to: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease
Highlights
Correction After the publication of this work [1] it was brought to the authors attention that Table three (Table 1 here) stated that the patient with Charcot-Marie-Tooth disease had scoliosis, when the patient did not have scoliosis
Yes Yes Yes Yes Proximal = distal No Yes No No No Yes Yes Yes (60%) Yes (80%) Motor neuropathy Muscle denervation Normal
We regret any inconvenience that this inaccuracy may have caused
Summary
Correction After the publication of this work [1] it was brought to the authors attention that Table three (Table 1 here) stated that the patient with Charcot-Marie-Tooth disease had scoliosis, when the patient did not have scoliosis. * Correspondence: kwchung@kongju.ac.kr; bochoi@ewha.ac.kr †Equal contributors 2Department of Biological Science, Kongju National University, 182 Sinkwandong, Gongju 314-701, Korea 1Department of Neurology, School of Medicine, Ewha Womans University, 911-1 Mokdong, Yangcheon-ku, Seoul 158-710, Korea Disease Phenotype Origin Mutation Nucleotide change Amino acid change Age at onset Symptom at onset Muscle weakness
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