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8. The shifting paradigm of Charcot-Marie-Tooth disease. Echaniz-Laguna A Rev Neurol (Paris); 2015; 171(6-7):498-504. PubMed ID: 25896909 [TBL] [Abstract][Full Text] [Related]
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19. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations. Chung KW; Kim SB; Park KD; Choi KG; Lee JH; Eun HW; Suh JS; Hwang JH; Kim WK; Seo BC; Kim SH; Son IH; Kim SM; Sunwoo IN; Choi BO Brain; 2006 Aug; 129(Pt 8):2103-18. PubMed ID: 16835246 [TBL] [Abstract][Full Text] [Related]
20. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group. Raeymaekers P; Timmerman V; Nelis E; De Jonghe P; Hoogendijk JE; Baas F; Barker DF; Martin JJ; De Visser M; Bolhuis PA Neuromuscul Disord; 1991; 1(2):93-7. PubMed ID: 1822787 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]