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Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
Bernkopf, Marie; Webersinke, Gerald; Tongsook, Chanakan; Koyani, Chintan N; Rafiq, Muhammad A; Ayaz, Muhammad; Müller, Doris; Enzinger, Christian; Aslam, Muhammad; Naeem, Farooq; Schmidt, Kurt; Gruber, Karl; Speicher, Michael R; Malle, Ernst; Macheroux, Peter; Ayub, Muhammad; Vincent, John B; Windpassinger, Christian; Duba, Hans-Christoph.
Afiliação
  • Bernkopf M; Laboratory of Molecular Biology and Tumorcytogenetics, Department of Internal Medicine, Krankenhaus der Barmherzigen Schwestern, Linz, Austria.
  • Webersinke G; Laboratory of Molecular Biology and Tumorcytogenetics, Department of Internal Medicine, Krankenhaus der Barmherzigen Schwestern, Linz, Austria.
  • Tongsook C; Institute of Biochemistry, Graz University of Technology, Graz, Austria.
  • Koyani CN; Institute of Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria.
  • Rafiq MA; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Brain Research Institute, The Centre for Addiction & Mental Health (CAMH), Toronto, ON, Canada.
  • Ayaz M; Lahore Institute of Research and Development, Lahore, Punjab Province, Pakistan.
  • Müller D; Department of Human Genetics, Landes-Frauen und Kinderklinik, Linz, Austria.
  • Enzinger C; Department of Neurology and.
  • Aslam M; Lahore Institute of Research and Development, Lahore, Punjab Province, Pakistan.
  • Naeem F; Lahore Institute of Research and Development, Lahore, Punjab Province, Pakistan Division of Developmental Disabilities, Department of Psychiatry, Queen's University, Kingston, ON, Canada.
  • Schmidt K; Department of Pharmacology and Toxicology, Karl-Franzens University Graz, Graz, Austria.
  • Gruber K; Institute of Molecular Biosciences, University of Graz, Graz, Austria.
  • Speicher MR; Institute of Human Genetics, Medical University of Graz, Graz, Austria.
  • Malle E; Institute of Molecular Biology and Biochemistry, Medical University of Graz, Graz, Austria.
  • Macheroux P; Institute of Biochemistry, Graz University of Technology, Graz, Austria.
  • Ayub M; Lahore Institute of Research and Development, Lahore, Punjab Province, Pakistan Division of Developmental Disabilities, Department of Psychiatry, Queen's University, Kingston, ON, Canada.
  • Vincent JB; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Brain Research Institute, The Centre for Addiction & Mental Health (CAMH), Toronto, ON, Canada Department of Psychiatry and Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Windpassinger C; Institute of Human Genetics, Medical University of Graz, Graz, Austria christian.windpassinger@medunigraz.at.
  • Duba HC; Department of Human Genetics, Landes-Frauen und Kinderklinik, Linz, Austria.
Hum Mol Genet ; 23(15): 4015-23, 2014 Aug 01.
Article em En | MEDLINE | ID: mdl-24626631
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual / Metiltransferases / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Áustria
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual / Metiltransferases / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Áustria