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Chromosomal rearrangements
Original article
CTNND2—a candidate gene for reading problems and mild intellectual disability

Authors

  • Wolfgang Hofmeister Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Daniel Nilsson Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden Science for Life Laboratory, Karolinska Institutet Science Park, Solna, Sweden PubMed articlesGoogle scholar articles
  • Alexandra Topa Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden PubMed articlesGoogle scholar articles
  • Britt-Marie Anderlid Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Fahimeh Darki Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Hans Matsson Department of Biosciences and Nutrition, Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden PubMed articlesGoogle scholar articles
  • Isabel Tapia Páez Department of Biosciences and Nutrition, Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden PubMed articlesGoogle scholar articles
  • Torkel Klingberg Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Lena Samuelsson Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden PubMed articlesGoogle scholar articles
  • Valtteri Wirta SciLifeLab, School of Biotechnology, KTH Royal Institute of Technology, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Francesco Vezzi SciLifeLab, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Juha Kere Department of Biosciences and Nutrition, Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden Molecular Neurology Research Program, University of Helsinki, and Folkhälsan Institute of Genetics, Helsinki, Finland PubMed articlesGoogle scholar articles
  • Magnus Nordenskjöld Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Elisabeth Syk Lundberg Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden PubMed articlesGoogle scholar articles
  • Anna Lindstrand Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Anna Lindstrand, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm S-171 76, Sweden; Anna.Lindstrand{at}ki.se
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Citation

Hofmeister W, Nilsson D, Topa A, et al
CTNND2—a candidate gene for reading problems and mild intellectual disability
Journal of Medical Genetics 2015;52:111-122.

Publication history

  • Received September 17, 2014
  • Revised October 31, 2014
  • Accepted November 12, 2014
  • First published December 3, 2014.
Online issue publication 
November 18, 2016

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