Title: Isolated generalized dystonia in biallelic missense mutations of the <i>ATM</i> gene
Abstract: Movement DisordersVolume 28, Issue 13 p. 1897-1899 Letters: New Observation Isolated generalized dystonia in biallelic missense mutations of the ATM gene Wassilios G. Meissner MD, PhD, Corresponding Author Wassilios G. Meissner MD, PhD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, France Institut des Maladies Neurodégénératives, Unité Mixte de Recherche (UMR) 5293, University de Bordeaux, Bordeaux, France Le Centre National de la Recherche Scientifique, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France Wassilios G. Meissner and Marie Fernet contributed equally to this work.Correspondence to: Prof. W. Meissner Department of Neurology, University Hospital Bordeaux, Avenue Magellan, 33604 Pessac Cedex, France; [email protected]Search for more papers by this authorMarie Fernet PhD, Marie Fernet PhD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, France Wassilios G. Meissner and Marie Fernet contributed equally to this work.Search for more papers by this authorJérôme Couturier MD, Jérôme Couturier MD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, FranceSearch for more papers by this authorJanet Hall PhD, Janet Hall PhD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, FranceSearch for more papers by this authorAnthony Laugé PhD, Anthony Laugé PhD Institut Curie, Department of Tumour Biology, Paris, FranceSearch for more papers by this authorPatrick Henry MD, Patrick Henry MD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, FranceSearch for more papers by this authorDominique Stoppa-Lyonnet MD, PhD, Dominique Stoppa-Lyonnet MD, PhD Institut Curie, Department of Tumour Biology, Paris, France Institut Curie, INSERM Unité 830, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, FranceSearch for more papers by this authorFrançois Tison MD, PhD, François Tison MD, PhD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, France Institut des Maladies Neurodégénératives, Unité Mixte de Recherche (UMR) 5293, University de Bordeaux, Bordeaux, France Le Centre National de la Recherche Scientifique, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, FranceSearch for more papers by this author Wassilios G. Meissner MD, PhD, Corresponding Author Wassilios G. Meissner MD, PhD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, France Institut des Maladies Neurodégénératives, Unité Mixte de Recherche (UMR) 5293, University de Bordeaux, Bordeaux, France Le Centre National de la Recherche Scientifique, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France Wassilios G. Meissner and Marie Fernet contributed equally to this work.Correspondence to: Prof. W. Meissner Department of Neurology, University Hospital Bordeaux, Avenue Magellan, 33604 Pessac Cedex, France; [email protected]Search for more papers by this authorMarie Fernet PhD, Marie Fernet PhD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, France Wassilios G. Meissner and Marie Fernet contributed equally to this work.Search for more papers by this authorJérôme Couturier MD, Jérôme Couturier MD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, FranceSearch for more papers by this authorJanet Hall PhD, Janet Hall PhD Institut National de la Santé et de la Recherche Méedicale (INSERM) Unité 612, Orsay, France Institut Curie-Recherche, Orsay, FranceSearch for more papers by this authorAnthony Laugé PhD, Anthony Laugé PhD Institut Curie, Department of Tumour Biology, Paris, FranceSearch for more papers by this authorPatrick Henry MD, Patrick Henry MD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, FranceSearch for more papers by this authorDominique Stoppa-Lyonnet MD, PhD, Dominique Stoppa-Lyonnet MD, PhD Institut Curie, Department of Tumour Biology, Paris, France Institut Curie, INSERM Unité 830, Paris, France Université Paris Descartes, Sorbonne Paris Cité, Paris, FranceSearch for more papers by this authorFrançois Tison MD, PhD, François Tison MD, PhD Service de Neurologie, Centre Expert Parkinson et Centre Maladie Rare Atrophie Multisystématisée, Centre Hospitalier Universitaire de Bordeaux, Pessac, France Institut des Maladies Neurodégénératives, Unité Mixte de Recherche (UMR) 5293, University de Bordeaux, Bordeaux, France Le Centre National de la Recherche Scientifique, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, FranceSearch for more papers by this author First published: 02 May 2013 https://doi.org/10.1002/mds.25487Citations: 17 Relevant conflicts of interest/financial disclosures: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article.Citing Literature Supporting Information Additional Supporting Information may be found in the online version of this article. Filename Description mds25487-sup-0001-suppinfo.wmv20.3 MB Supplementary Information Video mds25487-sup-0002-suppinfo.doc359.5 KB Supporting Information Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. Volume28, Issue13November 2013Pages 1897-1899 RelatedInformation
Publication Year: 2013
Publication Date: 2013-05-02
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 23
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