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14. Early clinical and electrophysiologic features of the two most common autosomal recessive forms of Charcot-Marie-Tooth disease in the Roma (Gypsies). Guergueltcheva V; Tournev I; Bojinova V; Hantke J; Litvinenko I; Ishpekova B; Shmarov A; Petrova J; Jordanova A; Kalaydjieva L J Child Neurol; 2006 Jan; 21(1):20-5. PubMed ID: 16551448 [TBL] [Abstract][Full Text] [Related]
15. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation]. Ohnishi A; Yoshimura T; Takazawa A; Hashimoto T; Yamamoto T; Fukushima Y Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724 [TBL] [Abstract][Full Text] [Related]
16. [A case of hereditary motor and sensory neuropathy of neuronal type with retardation of motor development]. Nakano S; Ohnishi A; Yamamoto T; Oishi T; Murai Y Rinsho Shinkeigaku; 1990 Apr; 30(4):448-51. PubMed ID: 2387117 [TBL] [Abstract][Full Text] [Related]
17. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness]. Fukuda H; Kitani M; Imaoka K Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389 [TBL] [Abstract][Full Text] [Related]
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20. The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4. Claramunt R; Sevilla T; Lupo V; Cuesta A; Millán JM; Vílchez JJ; Palau F; Espinós C Clin Genet; 2007 Apr; 71(4):343-9. PubMed ID: 17470135 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]