DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA-Reference-Cited by-同舟云学术

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

Published:2008-03 Issue:3 Volume:7 Page:207-215
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Camargos Sarah,Scholz Sonja,Simón-Sánchez Javier,Paisán-Ruiz Coro,Lewis Patrick,Hernandez Dena,Ding Jinhui,Gibbs J Raphael,Cookson Mark R,Bras Jose,Guerreiro Rita,Oliveira Catarina Resende,Lees Andrew,Hardy John,Cardoso Francisco,Singleton Andrew B

Publisher

Elsevier BV

Subject

Neurology (clinical)

Reference19 articles.

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2. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene;Ichinose;Nat Genet,1994

3. Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism;Nolte;Proc Natl Acad Sci USA,2003

4. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein;Ozelius;Nat Genet,1997

5. Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis;Rainier;Arch Neurol,2004

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