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CTNND2-a candidate gene for reading problems and mild intellectual disability.
Hofmeister, Wolfgang; Nilsson, Daniel; Topa, Alexandra; Anderlid, Britt-Marie; Darki, Fahimeh; Matsson, Hans; Tapia Páez, Isabel; Klingberg, Torkel; Samuelsson, Lena; Wirta, Valtteri; Vezzi, Francesco; Kere, Juha; Nordenskjöld, Magnus; Syk Lundberg, Elisabeth; Lindstrand, Anna.
Afiliación
  • Hofmeister W; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Nilsson D; 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
  • Topa A; Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Anderlid BM; 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.
  • Darki F; Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Matsson H; Department of Biosciences and Nutrition, Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Tapia Páez I; Department of Biosciences and Nutrition, Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Klingberg T; Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
  • Samuelsson L; Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Wirta V; SciLifeLab, School of Biotechnology, KTH Royal Institute of Technology, Stockholm, Sweden.
  • Vezzi F; SciLifeLab, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
  • Kere J; 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.
  • Nordenskjöld M; 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.
  • Syk Lundberg E; 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.
  • Lindstrand A; 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.
J Med Genet ; 52(2): 111-22, 2015 Feb.
Article en En | MEDLINE | ID: mdl-25473103
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lectura / Predisposición Genética a la Enfermedad / Cateninas / Estudios de Asociación Genética / Discapacidad Intelectual Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lectura / Predisposición Genética a la Enfermedad / Cateninas / Estudios de Asociación Genética / Discapacidad Intelectual Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article