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Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population

Authors

  • Katherine Johnson John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Willem De Ridder Neurogenetics Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Ana Töpf John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Marta Bertoli John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Lauren Phillips John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Peter De Jonghe Neurogenetics Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Jonathan Baets Neurogenetics Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Tine Deconinck Neurogenetics Group, Center for Molecular Neurology, VIB, Antwerp, Belgium Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium PubMed articlesGoogle scholar articles
  • Vidosava Rakocevic Stojanovic Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia PubMed articlesGoogle scholar articles
  • Stojan Perić Neurology Clinic, Clinical Center of Serbia, School of Medicine, University of Belgrade, Belgrade, Serbia PubMed articlesGoogle scholar articles
  • Hacer Durmus Department of Neurology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey PubMed articlesGoogle scholar articles
  • Shirin Jamal-Omidi Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran PubMed articlesGoogle scholar articles
  • Shahriar Nafissi Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran PubMed articlesGoogle scholar articles
  • Tiziana Mongini Department of Neurosciences ‘Rita Levi Montalcini’, University of Turin, Turin, Italy PubMed articlesGoogle scholar articles
  • Anna Łusakowska Department of Neurology, Medical University of Warsaw, Warsaw, Poland PubMed articlesGoogle scholar articles
  • Mark Busby Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UK PubMed articlesGoogle scholar articles
  • James Miller The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Fiona Norwood King’s College Hospital, London, UK PubMed articlesGoogle scholar articles
  • Judith Hudson Northern Molecular Genetics Service, Biomedicine East Wing, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Rita Barresi John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK Muscle Immunoanalysis Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  • Monkol Lek Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Daniel G MacArthur Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Volker Straub John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Volker Straub, The John Walton Muscular Dystrophy Research Centre, MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, Newcastle upon Tyne, NE1 3BZ, UK; volker.straub{at}ncl.ac.uk
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Citation

Johnson K, De Ridder W, Töpf A, et al
Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population

Publication history

  • Received February 22, 2018
  • Revised May 24, 2018
  • Accepted May 29, 2018
  • First published June 19, 2018.
Online issue publication 
April 09, 2019

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