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Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson, Hans; Huss, Mikael; Persson, Helena; Einarsdottir, Elisabet; Tiraboschi, Ettore; Nopola-Hemmi, Jaana; Schumacher, Johannes; Neuhoff, Nina; Warnke, Andreas; Lyytinen, Heikki; Schulte-Körne, Gert; Nöthen, Markus M; Leppänen, Paavo H T; Peyrard-Janvid, Myriam; Kere, Juha.
Afiliação
  • Matsson H; Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Huss M; 1] Science for Life Laboratory, Stockholm, Sweden [2] Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
  • Persson H; Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Einarsdottir E; Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Tiraboschi E; Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Nopola-Hemmi J; Division of Child Neurology, Department of Gynecology and Pediatrics, Jorvi Hospital, University Central Hospital, Espoo, Finland.
  • Schumacher J; Institute of Human Genetics and Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.
  • Neuhoff N; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Munich, Munich, Germany.
  • Warnke A; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Wuerzburg, Wuerzburg, Germany.
  • Lyytinen H; Department of Psychology and Child Research Center, University of Jyväskylä, Jyväskylä, Finland.
  • Schulte-Körne G; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Munich, Munich, Germany.
  • Nöthen MM; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
  • Leppänen PH; Department of Psychology, University of Jyväskylä, Jyväskylä, Finland.
  • Peyrard-Janvid M; Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Kere J; 1] Department of Biosciences and Nutrition, and Center for Innovative Medicine, Karolinska Institutet, Huddinge, Sweden [2] Science for Life Laboratory, Stockholm, Sweden [3] Molecular Neurology Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland [4] Folkhälsan Instit
J Hum Genet ; 60(7): 399-401, 2015 Jul.
Article em En | MEDLINE | ID: mdl-25877001
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dislexia / Subunidade beta da Proteína Ligante de Cálcio S100 / Proteínas Associadas aos Microtúbulos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dislexia / Subunidade beta da Proteína Ligante de Cálcio S100 / Proteínas Associadas aos Microtúbulos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia País de publicação: Reino Unido