De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease. Motley WW, Palaima P, Yum SW, Gonzalez MA, Tao F, Wanschitz JV, Strickland AV, Löscher WN, De Vriendt E, Koppi S, et al. Brain. 2016 Mar 23. PMID: 27009151. Abstract CommentRecommendBookmarkWatch