A novel mutation of myelin protein zero associated with late-onset predominantly axonal Charcot-Marie-Tooth disease




MARTTILA M, RAUTENSTRAUSS B, Huehne K, Laitinen V, MAJAMAA K, Karppa M

2012

Journal of Neurology

8

259

8

1585

1589

5

0340-5354

DOIhttps://doi.org/10.1007/s00415-011-6382-5




Last updated on 2024-26-11 at 16:06