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Charcot-Marie-Tooth disease type 1A is the most common inherited neuropathy and is caused by duplication of chromosome 17p11.2 containing the peripheral myelin protein-22 gene. This disease is… (More)
Sir, We would like to make a few considerations on the recent paper published in Brain by Saporta et al. (2009), since our research focus in the recent years has been on quantification and… (More)