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TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.
Caubit, Xavier; Gubellini, Paolo; Andrieux, Joris; Roubertoux, Pierre L; Metwaly, Mehdi; Jacq, Bernard; Fatmi, Ahmed; Had-Aissouni, Laurence; Kwan, Kenneth Y; Salin, Pascal; Carlier, Michèle; Liedén, Agne; Rudd, Eva; Shinawi, Marwan; Vincent-Delorme, Catherine; Cuisset, Jean-Marie; Lemaitre, Marie-Pierre; Abderrehamane, Fatimetou; Duban, Bénédicte; Lemaitre, Jean-François; Woolf, Adrian S; Bockenhauer, Detlef; Severac, Dany; Dubois, Emeric; Zhu, Ying; Sestan, Nenad; Garratt, Alistair N; Lydia Kerkerian-Le, Goff; Fasano, Laurent.
  • Caubit X; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Gubellini P; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Andrieux J; Institut de génétique médicale, Hôpital Jeanne de Flandre, CHRU Lille, France.
  • Roubertoux PL; Aix Marseille Univ, INSERM, GMGF, Marseille, France.
  • Metwaly M; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Jacq B; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Fatmi A; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Had-Aissouni L; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Kwan KY; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Salin P; Molecular & Behavioral Neuroscience Institute (MBNI), Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA.
  • Carlier M; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
  • Liedén A; Aix Marseille Univ, CNRS, LPC, Marseille, France.
  • Rudd E; Karolinska University Hospital Solna, Clinical Genetics Unit, Stockholm, Sweden.
  • Shinawi M; Karolinska University Hospital Solna, Clinical Genetics Unit, Stockholm, Sweden.
  • Vincent-Delorme C; Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO, USA.
  • Cuisset JM; Service de Génétique clinique, Hôpital Jeanne de Flandre, CHRU Lille, France.
  • Lemaitre MP; Service de Neuropédiatrie, Hôpital Salengro, CHRU Lille, France.
  • Abderrehamane F; Service de Neuropédiatrie, Hôpital Salengro, CHRU Lille, France.
  • Duban B; Institut de génétique médicale, Hôpital Jeanne de Flandre, CHRU Lille, France.
  • Lemaitre JF; Centre de cytogénétique, Hôpital Saint Vincent de Paul, GHICL, UCL, Lille, France.
  • Woolf AS; Centre de cytogénétique, Hôpital Saint Vincent de Paul, GHICL, UCL, Lille, France.
  • Bockenhauer D; Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre and the Royal Manchester Children's and St Mary's Hospitals, Manchester, UK.
  • Severac D; UCL Institute of Child Health, London, UK.
  • Dubois E; MGX-Montpellier GenomiX, c/o Institut de Génomique Fonctionnelle, Montpellier, France.
  • Zhu Y; MGX-Montpellier GenomiX, c/o Institut de Génomique Fonctionnelle, Montpellier, France.
  • Sestan N; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Garratt AN; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Lydia Kerkerian-Le Goff; Institute of Cell Biology and Neurobiology, Center for Anatomy, Charité University Hospital Berlin, Berlin, Germany.
  • Fasano L; Aix Marseille Univ, CNRS, IBDM, Marseille, France.
Nat Genet ; 48(11): 1359-1369, 2016 11.
Article en En | MEDLINE | ID: mdl-27668656
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio / Neocórtex / Trastorno del Espectro Autista / Neuronas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Homeodominio / Neocórtex / Trastorno del Espectro Autista / Neuronas Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article