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Journal of the Neurological Sciences, ISSN 0022-510X, 11/2019, Volume 406, p. 116376
The autosomal recessive demyelinating form of Charcot-Marie-Tooth can be due to gene pathogenic variants (CMT4C, AR-CMTde- ). We report on a series of 13... 
Charcot-Marie-Tooth | Neuropathy | NGS | SH3TC2 | Scoliosis | Hearing loss
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