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Genotype-phenotype correlations
Original article
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1

Authors

  • John H Livingston Department of Paediatric Neurology, Leeds General Infirmary, Leeds, UK PubMed articlesGoogle scholar articles
  • Jean-Pierre Lin General Neurology & Complex Motor Disorders Service, Evelina Children's Neurosciences Centre, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK PubMed articlesGoogle scholar articles
  • Russell C Dale TY Nelson Department of Neurology, and Neuroimmunology group, The Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia PubMed articlesGoogle scholar articles
  • Deepak Gill TY Nelson Department of Neurology, and Neuroimmunology group, The Children's Hospital at Westmead, University of Sydney, Sydney, New South Wales, Australia PubMed articlesGoogle scholar articles
  • Paul Brogan Department of Paediatric Rheumatology, University College London, Institute of Child Health, London, UK Great Ormond Street Hospital NHS Foundation Trust, London, UK PubMed articlesGoogle scholar articles
  • Arnold Munnich Departement de Génétique, INSERM U781, Université Paris Descartes-Sorbonne Paris Cité, Institut Imagine, Hôpital Necker-Enfants Malades (AP-HP), Paris, France PubMed articlesGoogle scholar articles
  • Manju A Kurian Department of Neurology, Great Ormond Street Hospital NHS Foundation Trust, London, UK Neurosciences Unit, Institute of Child Health, University College London, London, UK PubMed articlesGoogle scholar articles
  • Victoria Gonzalez-Martinez Department of Neurosurgery, Hôpital Gui de Chauliac, University Hospital of Montpellier, Montpellier, France PubMed articlesGoogle scholar articles
  • Christian G E L De Goede Department of Paediatric Neurology, Royal Preston Hospital, Preston, UK PubMed articlesGoogle scholar articles
  • Alastair Falconer Department of Paediatrics, Scarborough General Hospital, Scarborough, UK PubMed articlesGoogle scholar articles
  • Gabriella Forte Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articlesGoogle scholar articles
  • Emma M Jenkinson Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articlesGoogle scholar articles
  • Paul R Kasher Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articlesGoogle scholar articles
  • Marcin Szynkiewicz Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articlesGoogle scholar articles
  • Gillian I Rice Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK PubMed articlesGoogle scholar articles
  • Yanick J Crow Department of Genetic Medicine, Faculty of Medical and Human Sciences, Institute of Human Development, University of Manchester, Manchester, UK Manchester Academic Health Science Centre, Central Manchester University Hospitals NHS Foundation Trust, St. Mary's Hospital, Manchester, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Y J Crow, Department of Genetic Medicine, University of Manchester, St Mary's Hospital, 6th Floor, Oxford Road, Manchester M13 9WL, UK; yanickcrow{at}mac.com
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Citation

Livingston JH, Lin J, Dale RC, et al
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1
Journal of Medical Genetics 2014;51:76-82.

Publication history

  • Received September 6, 2013
  • Revised October 18, 2013
  • Accepted October 21, 2013
  • First published November 21, 2013.
Online issue publication 
April 27, 2016

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