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1. Genetic and clinical characteristics of -related Charcot-Marie-Tooth disease.

2. Charcote-Mariee-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.

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3. Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2.

4. Genetic and clinical characteristics of NEFL -related Charcot-Marie-Tooth disease.

5. Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy.

6. Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation.