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9. Inherited and de novo mutations in sporadic cases of DYT1-dystonia. Hjermind LE, Werdelin LM, Sørensen SA. Eur J Hum Genet; 2002 Mar; 10(3):213-6. PubMed ID: 11973627 [Abstract] [Full Text] [Related]
10. Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystonia. Gambarin M, Valente EM, Liberini P, Barrano G, Bonizzato A, Padovani A, Moretto G, Fiorio M, Dallapiccola B, Smania N, Fiaschi A, Tinazzi M. Mov Disord; 2006 Oct; 21(10):1782-4. PubMed ID: 16874761 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
13. Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia. Grundmann K, Laubis-Herrmann U, Bauer I, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O. Arch Neurol; 2003 Sep; 60(9):1266-70. PubMed ID: 12975293 [Abstract] [Full Text] [Related]
14. Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation. Bressman SB, de Leon D, Kramer PL, Ozelius LJ, Brin MF, Greene PE, Fahn S, Breakefield XO, Risch NJ. Ann Neurol; 1994 Nov; 36(5):771-7. PubMed ID: 7979224 [Abstract] [Full Text] [Related]
15. Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature. Edwards M, Wood N, Bhatia K. Mov Disord; 2003 Jun; 18(6):706-11. PubMed ID: 12784278 [Abstract] [Full Text] [Related]