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Original article
SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome

Authors

  • Anna Schossig Division of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria PubMed articlesGoogle scholar articles
  • Agnès Bloch-Zupan Faculté de Chirurgie Dentaire, Université de Strasbourg, Strasbourg, France Pôle de Médecine et Chirurgie Bucco-dentaires, Centre de Référence des Manifestations Odontologiques des Maladies Rares, Hôpitaux Universitaires de Strasbourg (HUS), Strasbourg, France Institut de Génétique et de Biologie Moléculaire and Cellulaire-Centre Européen de Recherche en Biologie et en Médecine, Université de Strasbourg, IGBMC-CERBM CNRS UMR7104, INSERM U964, Illkirch, France PubMed articlesGoogle scholar articles
  • Adrian Lussi Department of Preventive, Restorative and Pediatric Dentistry, School of Dental Medicine, University of Bern, Bern, Switzerland PubMed articlesGoogle scholar articles
  • Nicole I Wolf Department of Child Neurology, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands PubMed articlesGoogle scholar articles
  • Salmo Raskin Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Brazil Genetika-Centro de Aconselhamento e Laboratório de Genética, Curitiba, Brazil PubMed articlesGoogle scholar articles
  • Monika Cohen kbo-Kinderzentrum München gGmbH, Munich, Germany PubMed articlesGoogle scholar articles
  • Fabienne Giuliano Centre de Référence Anomalies du Développement et Syndromes Malformatifs PACA, Service de Génétique Médicale, CHU Nice, Nice, France PubMed articlesGoogle scholar articles
  • Julie Jurgens McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA PubMed articlesGoogle scholar articles
  • Birgit Krabichler Division of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria PubMed articlesGoogle scholar articles
  • David A Koolen Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Nara Lygia de Macena Sobreira McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA PubMed articlesGoogle scholar articles
  • Elisabeth Maurer Division of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria PubMed articlesGoogle scholar articles
  • Michèle Muller-Bolla UFR Odontologie, Département d'Odontologie Pédiatrique, Université de Nice Sophia-Antipolis, UCA, Nice, France CHU de Nice, Pôle Odontologie, UF soins pour enfants; Laboratory URB2i—EA 4462, Paris Descartes, France PubMed articlesGoogle scholar articles
  • Johann Penzien Department of Neuropaediatrics, Klinikum Augsburg, Augsburg, Germany PubMed articlesGoogle scholar articles
  • Johannes Zschocke Division of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria PubMed articlesGoogle scholar articles
  • Ines Kapferer-Seebacher Department of Operative and Restorative Dentistry, Medical University of Innsbruck, Innsbruck, Austria PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Ines Kapferer-Seebacher, Department of Operative and Restorative Dentistry, Medical University of Innsbruck, Anichstraße 35, Innsbruck A-6020, Austria; ines.kapferer{at}i-med.ac.at
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Citation

Schossig A, Bloch-Zupan A, Lussi A, et al
SLC13A5 is the second gene associated with Kohlschütter–Tönz syndrome

Publication history

  • Received May 18, 2016
  • Revised July 12, 2016
  • Accepted August 1, 2016
  • First published September 6, 2016.
Online issue publication 
December 14, 2016

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