Emerging common molecular pathways for primary dystonia-Reference-Cited by-同舟云学术

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Emerging common molecular pathways for primary dystonia

Published:2013-06-15 Issue:7 Volume:28 Page:968-981
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

LeDoux Mark S.¹,Dauer William T.²,Warner Thomas T.³

Affiliation:

1. Department of Neurology; University of Tennessee Health Science Center Memphis; Tennessee 38163 USA

2. Department of Neurology and Cell & Developmental Biology; University of Michigan Medical School; Ann Arbor Michigan USA

3. Reta Lila Weston Institute for Neurological Research, UCL Institute of Neurology; London United Kingdom

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25547/fullpdf

Reference132 articles.

1. Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis;Phukan;Lancet Neurol.,2011

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

3. AAA+ proteins: have engine will work;Hanson;Nat Rev Mol Cell. Biol,2005

4. Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier;Kock;Hum Mol Genet.,2006

5. Expression of the early onset torsion dystonia gene (DYT1) in human brain;Augood;Ann Neurol.,1998

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4. Structural and functional brain abnormalities in idiopathic cervical dystonia: A multimodal meta-analysis;Parkinsonism & Related Disorders;2022-10

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