Chapter 37 Charcot-Marie-Tooth disease and related disorders
Author:
Funder
Muscular Dystrophy Association
National Institutes of Health
National Institute of Neurological Disorders and Stroke
Publisher
Elsevier
Reference151 articles.
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2. Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies;Anderson;Neurology,2000
3. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V;Antonellis;Am. J. Hum. Genet.,2003
4. Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I;Aramideh;J. Neurol.,1992
5. Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene;Azzedine;Neuromuscul. Disord.,2003
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