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Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset.
Mirza-Schreiber, Nazanin; Zech, Michael; Wilson, Rory; Brunet, Theresa; Wagner, Matias; Jech, Robert; Boesch, Sylvia; Skorvánek, Matej; Necpál, Ján; Weise, David; Weber, Sandrina; Mollenhauer, Brit; Trenkwalder, Claudia; Maier, Esther M; Borggraefe, Ingo; Vill, Katharina; Hackenberg, Annette; Pilshofer, Veronika; Kotzaeridou, Urania; Schwaibold, Eva Maria Christina; Hoefele, Julia; Waldenberger, Melanie; Gieger, Christian; Peters, Annette; Meitinger, Thomas; Schormair, Barbara; Winkelmann, Juliane; Oexle, Konrad.
Afiliação
  • Mirza-Schreiber N; Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Zech M; Neurogenetic Systems Analysis Group, Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Wilson R; Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Brunet T; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675 Munich, Germany.
  • Wagner M; Research Unit Molecular Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Jech R; Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Boesch S; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675 Munich, Germany.
  • Skorvánek M; Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Necpál J; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675 Munich, Germany.
  • Weise D; Department of Neurology, Charles University, 1st Faculty of Medicine and General University Hospital in Prague, 121 08 Prague, Czech Republic.
  • Weber S; Department of Neurology, Medizinische Universität, 6020 Insbruck, Austria.
  • Mollenhauer B; Department of Neurology, P. J. Safarik University, 04011 Kosice, Slovakia.
  • Trenkwalder C; Department of Neurology, University Hospital L. Pasteur, 04011 Kosice, Slovakia.
  • Maier EM; Department of Neurology, Zvolen Hospital, 96001 Zvolen, Slovakia.
  • Borggraefe I; Department of Neurology, Asklepios Fachklinikum Stadtroda, 07646 Stadtroda, Germany.
  • Vill K; Department of Neurology, University of Leipzig, 04103 Leipzig, Germany.
  • Hackenberg A; Institute of Neurogenomics (ING), Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Pilshofer V; University Medical Center Goettingen, Department of Neurology, Paracelsus-Elena-Klinik, 34128 Kassel, Germany.
  • Kotzaeridou U; University Medical Center Goettingen, Department of Neurology, Paracelsus-Elena-Klinik, 34128 Kassel, Germany.
  • Schwaibold EMC; University Medical Center Goettingen, Department of Neurology, Paracelsus-Elena-Klinik, 34128 Kassel, Germany.
  • Hoefele J; Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, 80337 Munich, Germany.
  • Waldenberger M; Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, 80337 Munich, Germany.
  • Gieger C; Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University, 80337 Munich, Germany.
  • Peters A; Department of Pediatric Neurology, University Children's Hospital, 8032 Zürich, Switzerland.
  • Meitinger T; Ordensklinikum Linz, Barmherzige Schwestern, 4010 Linz, Austria.
  • Schormair B; Department of Child Neurology and Metabolic Medicine, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, 69120 Heidelberg, Germany.
  • Winkelmann J; Institute of Human Genetics, Heidelberg University, 69120 Heidelberg, Germany.
  • Oexle K; Institute of Human Genetics, Technical University of Munich, School of Medicine, 81675 Munich, Germany.
Brain ; 145(2): 644-654, 2022 04 18.
Article em En | MEDLINE | ID: mdl-34590685
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distúrbios Distônicos / Distonia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distúrbios Distônicos / Distonia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha