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2) Herz E. Dystonia I. Historical review; analysis of dystonic symptoms and physiologic mechanisms involved. Arch Neurol Psychiatr. 1944; 51: 305-18
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3) Denny-Brown D. the basal ganglia and their relation to disorders of movement. Oxford Press. 1962. p. 78-80
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4) Fahn S, Marsden CD, Calne DB. Classification and investigation of dystonia. In: Marsden CD, Fahn S, editors. Movement Disorders. 2nd ed. London: Butterworths; 1987
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6) Gambarin M, Valente EM, Liverini P, et al. Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystonia. Mov Disord. 2006; 21: 1782-4
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7) Risch NJ, Bressman SB, Senthil G, et al. Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia. Am J Hum Genet. 2007; 80: 1188-93
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8) Ohta E, Funayama M, Ichinose H, et al. Novel Mutations in the Guanosine Triphosphate Cyclohydrolase 1 Gene Associated With DYT5 Dystonia. Arch Neurol. 2006; 63: 1605-10
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9) http://www.bh4.org/biodefdocs/gch1.pd
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10) Rainier S, Thomas D, Tokarz D, et al. Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis. Arch. Neurol. 2004; 61: 1025-9
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11) Tomita H, Nagamitsu S, Wakui K, et al. Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11. 2-q12. 1. Am J Hum Genet. 1999; 65: 1688-97
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14) Esapa CT, Waite A, Locke M, et al. SGCE missense mutations that cause myoclonus-dystonia syndrome impair ε-sarucoglycan trafficking to the plasma membrane moduration by ubiquitination and torsinA. Hum Mole Gent. 2007; 16: 327-42
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15) de Carvalho Aguiar P, Sweadner KJ, Penniston J, et al. Mutations in the Na(+)/K(+)-ATPase alpha-3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004; 43: 169-75
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18) Makino S, Kaji R, Ando S, et al. Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism. Am J Hum Genet. 2007; 80: 393-406
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