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Literature DB >> 16567727

Lack of association with TorsinA haplotype in German patients with sporadic dystonia.

S Hague¹, S Klaffke, J Clarimon, B Hemmer, A Singleton, A Kupsch, O Bandmann.

Abstract

Entities: Disease Gene Species

Mesh：

Substances：

Year: 2006 PMID： 16567727 DOI： 10.1212/01.wnl.0000203344.43342.18

Source DB: PubMed Journal: Neurology ISSN： 0028-3878 Impact factor: 9.910

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15 in total

Review 1. Genetic and clinical features of primary torsion dystonia.

Authors: Laurie J Ozelius; Susan B Bressman
Journal: Neurobiol Dis Date: 2010-12-17 Impact factor: 5.996

Review 2. Inherited isolated dystonia: clinical genetics and gene function.

Authors: William Dauer
Journal: Neurotherapeutics Date: 2014-10 Impact factor: 7.620

3. Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.

Authors: Subhajit Giri; Arunibha Ghosh; Shubhrajit Roy; Charulata Savant Sankhla; Shyamal Kumar Das; Kunal Ray; Jharna Ray
Journal: J Mol Neurosci Date: 2020-07-13 Impact factor: 3.444

4. Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.

Authors: Gary A Heiman; Ruth Ottman; Rachel J Saunders-Pullman; Laurie J Ozelius; Neil J Risch; Susan B Bressman
Journal: Am J Med Genet B Neuropsychiatr Genet Date: 2007-04-05 Impact factor: 3.568

5. An examination of TOR1A variants in recurrent major depression.

Authors: F Heining; B Langguth; P Eichhammer; Domani M; Hajak G; P G Sand
Journal: Int J Mol Epidemiol Genet Date: 2012-02-28

6. Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Authors: Nutan Sharma; Ramon A Franco; John K Kuster; Adele A Mitchell; Tania Fuchs; Rachel Saunders-Pullman; Deborah Raymond; Mitchell F Brin; Andrew Blitzer; Susan B Bressman; Laurie J Ozelius
Journal: Mov Disord Date: 2010-10-15 Impact factor: 10.338

Lack of association with TorsinA haplotype in German patients with sporadic dystonia.

Review 1. Genetic and clinical features of primary torsion dystonia.

Review 2. Inherited isolated dystonia: clinical genetics and gene function.

3. Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India.

4. Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.

5. An examination of TOR1A variants in recurrent major depression.

6. Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

7. Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia.

8. Dystonia-Causing Mutations as a Contribution to the Etiology of Spasmodic Dysphonia.

Review 9. Experimental therapeutics for dystonia.

10. Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia.