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10. [Recessive dopa-responsive form of dystonia due to a mutation of the tyrosine hydroxylase gene]. Rondot P; Wevers RA Bull Acad Natl Med; 1999; 183(3):639-46; discussion 646-7. PubMed ID: 10437291 [TBL] [Abstract][Full Text] [Related]
11. Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations. Kustedjo K; Bracey MH; Cravatt BF J Biol Chem; 2000 Sep; 275(36):27933-9. PubMed ID: 10871631 [TBL] [Abstract][Full Text] [Related]
12. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia. Slominsky PA; Markova ED; Shadrina MI; Illarioshkin SN; Miklina NI; Limborska SA; Ivanova-Smolenskaya IA Hum Mutat; 1999 Sep; 14(3):269. PubMed ID: 10477437 [TBL] [Abstract][Full Text] [Related]
13. Genetics and pharmacological treatment of dystonia. Barrett MJ; Bressman S Int Rev Neurobiol; 2011; 98():525-49. PubMed ID: 21907099 [TBL] [Abstract][Full Text] [Related]
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17. Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family. Holmgren G; Ozelius L; Forsgren L; Almay BG; Holmberg M; Kramer P; Fahn S; Breakefield XO J Neurol Neurosurg Psychiatry; 1995 Aug; 59(2):178-81. PubMed ID: 7629534 [TBL] [Abstract][Full Text] [Related]
18. Genetic and clinical features of primary torsion dystonia. Ozelius LJ; Bressman SB Neurobiol Dis; 2011 May; 42(2):127-35. PubMed ID: 21168499 [TBL] [Abstract][Full Text] [Related]
19. Expression of the early-onset torsion dystonia gene (DYT1) in human brain. Augood SJ; Penney JB; Friberg IK; Breakefield XO; Young AB; Ozelius LJ; Standaert DG Ann Neurol; 1998 May; 43(5):669-73. PubMed ID: 9585364 [TBL] [Abstract][Full Text] [Related]
20. Sensorimotor tests unmask a phenotype in the DYT1 knock-in mouse model of dystonia. Richter F; Gerstenberger J; Bauer A; Liang CC; Richter A Behav Brain Res; 2017 Jan; 317():536-541. PubMed ID: 27769743 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]