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26. [Charcot-Marie-Tooth (CMT) disease: an update]. Vallat JM; Funalot B Med Sci (Paris); 2010 Oct; 26(10):842-7. PubMed ID: 20929675 [TBL] [Abstract][Full Text] [Related]
27. Reliability and validity of the CMT neuropathy score as a measure of disability. Shy ME; Blake J; Krajewski K; Fuerst DR; Laura M; Hahn AF; Li J; Lewis RA; Reilly M Neurology; 2005 Apr; 64(7):1209-14. PubMed ID: 15824348 [TBL] [Abstract][Full Text] [Related]
28. [Different phenotypes of Charcot-Marie-Tooth disease caused by mutations in the same gene. Are classical criteria for classification still valid?]. Sevilla T; Vílchez JJ Neurologia; 2004 Jun; 19(5):264-71. PubMed ID: 15150710 [TBL] [Abstract][Full Text] [Related]
29. Molecular basis of axonal dysfunction and traffic impairments in CMT. Gentil BJ; Cooper L Brain Res Bull; 2012 Aug; 88(5):444-53. PubMed ID: 22595495 [TBL] [Abstract][Full Text] [Related]
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33. [Molecular basis of Charcot-Marie-Tooth neuropathy]. Hayasaka K Nihon Rinsho; 1996 Aug; 54(8):2243-51. PubMed ID: 8810804 [TBL] [Abstract][Full Text] [Related]
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35. [Molecular mechanisms of hereditary neuropathy: genotype-phenotype correlation]. Nakagawa M; Takashima H Rinsho Byori; 2003 Jun; 51(6):536-43. PubMed ID: 12884740 [TBL] [Abstract][Full Text] [Related]
36. Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. Stojkovic T; Latour P; Viet G; de Seze J; Hurtevent JF; Vandenberghe A; Vermersch P Neuromuscul Disord; 2004 Apr; 14(4):261-4. PubMed ID: 15019704 [TBL] [Abstract][Full Text] [Related]
37. Inherited neuropathies: new genes don't fit old models. Scherer SS Neuron; 2006 Sep; 51(6):672-4. PubMed ID: 16982409 [TBL] [Abstract][Full Text] [Related]
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