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




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