RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder
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Article Information
- Received October 1, 2014
- Accepted in final form January 16, 2015
- First Published April 3, 2015.
Article Versions
- Previous version (April 3, 2015 - 13:00).
- You are viewing the most recent version of this article.
Author Disclosures
- Patrick Santens, MD, PhD,
- Tim Van Damme, MD,
- Wouter Steyaert, BSc,
- Andy Willaert, PhD,
- Bernard Sablonnière, MD, PhD,
- Anne De Paepe, MD, PhD,
- Paul J. Coucke, PhD* and
- Bart Dermaut, MD, PhD*
- Patrick Santens, MD, PhD,
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Commercial : Grants by Lundbeck, Abbvie, Medtronic
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- Tim Van Damme, MD,
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- Wouter Steyaert, BSc,
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- Andy Willaert, PhD,
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- Bernard Sablonnière, MD, PhD,
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- Anne De Paepe, MD, PhD,
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- Paul J. Coucke, PhD* and
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- Bart Dermaut, MD, PhD*
non-profit entity
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PLoS One, Academic Editor since 2012
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University of Lille, University of Ghent
This study was supported by Inserm, the University of Lille 2, DN2M (D?mences des maladies Neurologiques et Mentales) as part of the contract project of the ? Etat R?gion Nord/Pas-de-Calais ? in France.
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- From the Department of Neurology (P.S., B.D.) and the Center for Medical Genetics (T.V.D., W.S., A.W., A.D.P., P.J.C., B.D.), Ghent University Hospital, Belgium; and Inserm U1172, Centre de Recherches J-P Aubert (B.S.), and Inserm U1167, Institut Pasteur de Lille (B.D.), Université de Lille, France.
- Correspondence to Dr. Dermaut: bart.dermaut{at}ugent.be
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