The association between multiple sclerosis (MS) and hereditary and sporadic demyelinating disorders of the peripheral nervous system is extremely rare. We herein report a case of Charcot-Marie-Tooth disease type 1B with p.Val102fs mutation in the MPZ gene that developed relapsing remitting MS.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167010 | PMC |
| http://dx.doi.org/10.1002/brb3.580 | DOI Listing |
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