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Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation

Authors

  • Estrella Gómez-Tortosa Department of Neurology, Fundación Jiménez Díaz, Madrid, Spain PubMed articlesGoogle scholar articles
  • Julie Van der Zee Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • María Ruggiero Department of Neurology, Fundación Jiménez Díaz, Madrid, Spain PubMed articlesGoogle scholar articles
  • Ilse Gijselinck Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Jesús Esteban-Pérez ALS Unit, 12 de Octubre Hospital Health Research Institute ’imas12', and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER U-723), Madrid, Spain PubMed articlesGoogle scholar articles
  • Alberto García-Redondo ALS Unit, 12 de Octubre Hospital Health Research Institute ’imas12', and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER U-723), Madrid, Spain PubMed articlesGoogle scholar articles
  • Daniel Borrego-Hernández ALS Unit, 12 de Octubre Hospital Health Research Institute ’imas12', and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER U-723), Madrid, Spain PubMed articlesGoogle scholar articles
  • Eloísa Navarro Department of Neurology, Hospital Infanta Leonor, Madrid, Spain PubMed articlesGoogle scholar articles
  • M. José Sainz Department of Neurology, Fundación Jiménez Díaz, Madrid, Spain PubMed articlesGoogle scholar articles
  • Julián Pérez-Pérez Department of Genetics, Secugen S.L., Madrid, Spain PubMed articlesGoogle scholar articles
  • Marc Cruts Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Christine Van Broeckhoven Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Rosa Guerrero-López Department of Neurology, Fundación Jiménez Díaz, Madrid, Spain Instituto de Investigaciones Sanitarias Fundación Jiménez Díaz (IIS-FJD) and Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain PubMed articlesGoogle scholar articles
  • on behalf of the EU EOD Consortium
    Google scholar articles
  1. Correspondence to Dr Estrella Gómez-Tortosa, Department of Neurology, Fundación Jiménez Díaz, Avda. Reyes Catolicos 2, Madrid 28040, Spain; egomezt{at}fjd.es
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Citation

Gómez-Tortosa E, Van der Zee J, Ruggiero M on behalf of the EU EOD Consortium, et al
Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation

Publication history

  • Received November 9, 2016
  • Revised February 1, 2017
  • Accepted March 1, 2017
  • First published April 1, 2017.
Online issue publication 
January 09, 2018

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