Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4). Piscosquito G, Saveri P, Magri S, Ciano C, Gandioli C, Morbin M, Di Bella D, Moroni I, Taroni F F, Pareyson D J Peripher Nerv Syst. 2016 May 27. PMID: 27231023. Abstract CommentRecommendBookmarkWatch
