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5. Genetic spectrum and clinical features in a cohort of Chinese patients with isolated dystonia. Li LX; Liu Y; Huang JH; Yang Y; Pan YG; Zhang XL; Pan LZ; Jin LJ Clin Genet; 2023 Apr; 103(4):459-465. PubMed ID: 36648081 [TBL] [Abstract][Full Text] [Related]
6. Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population. Wang L; Duan C; Gao Y; Xu W; Ding J; Liu VT; Wu Y Clin Neurol Neurosurg; 2016 Mar; 142():26-30. PubMed ID: 26803725 [TBL] [Abstract][Full Text] [Related]
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11. Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia. Cheng FB; Feng JC; Ma LY; Miao J; Ott T; Wan XH; Grundmann K Mov Disord; 2014 Jul; 29(8):1079-83. PubMed ID: 24862462 [TBL] [Abstract][Full Text] [Related]
12. The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6). Kaiser FJ; Osmanoric A; Rakovic A; Erogullari A; Uflacker N; Braunholz D; Lohnau T; Orolicki S; Albrecht M; Gillessen-Kaesbach G; Klein C; Lohmann K Ann Neurol; 2010 Oct; 68(4):554-9. PubMed ID: 20976771 [TBL] [Abstract][Full Text] [Related]
13. Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion. De Carvalho Aguiar P; Fuchs T; Borges V; Lamar KM; Silva SM; Ferraz HB; Ozelius L Mov Disord; 2010 Dec; 25(16):2854-7. PubMed ID: 20925076 [TBL] [Abstract][Full Text] [Related]
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15. Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function. Dos Santos CO; Masuho I; da Silva-Júnior FP; Barbosa ER; Silva SM; Borges V; Ferraz HB; Rocha MS; Limongi JC; Martemyanov KA; de Carvalho Aguiar P J Neurol; 2016 Apr; 263(4):665-8. PubMed ID: 26810727 [TBL] [Abstract][Full Text] [Related]
16. Risk Factor Genes in Patients with Dystonia: A Comprehensive Review. Siokas V; Aloizou AM; Tsouris Z; Michalopoulou A; Mentis AA; Dardiotis E Tremor Other Hyperkinet Mov (N Y); 2018; 8():559. PubMed ID: 30643666 [TBL] [Abstract][Full Text] [Related]
17. Update on the Genetics of Dystonia. Lohmann K; Klein C Curr Neurol Neurosci Rep; 2017 Mar; 17(3):26. PubMed ID: 28283962 [TBL] [Abstract][Full Text] [Related]
18. Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia. Dobričić VS; Kresojević ND; Svetel MV; Janković MZ; Petrović IN; Tomić AD; Novaković IV; Kostić VS J Neurol; 2013 Apr; 260(4):1037-42. PubMed ID: 23180184 [TBL] [Abstract][Full Text] [Related]
19. Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia. da Silva-Junior FP; dos Santos CO; Silva SM; Barbosa ER; Borges V; Ferraz HB; Limongi JC; Rocha MS; de Carvalho Aguiar P J Neurol Sci; 2014 Sep; 344(1-2):190-2. PubMed ID: 24976531 [TBL] [Abstract][Full Text] [Related]
20. Mutation screening of GNAL gene in patients with primary dystonia from Northeast China. Miao J; Wan XH; Sun Y; Feng JC; Cheng FB Parkinsonism Relat Disord; 2013 Oct; 19(10):910-2. PubMed ID: 23759320 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]