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Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.
Fogel, Brent L; Cho, Ellen; Wahnich, Amanda; Gao, Fuying; Becherel, Olivier J; Wang, Xizhe; Fike, Francesca; Chen, Leslie; Criscuolo, Chiara; De Michele, Giuseppe; Filla, Alessandro; Collins, Abigail; Hahn, Angelika F; Gatti, Richard A; Konopka, Genevieve; Perlman, Susan; Lavin, Martin F; Geschwind, Daniel H; Coppola, Giovanni.
Afiliación
  • Fogel BL; Program in Neurogenetics, Department of Neurology and bfogel@ucla.edu.
  • Cho E; Program in Neurogenetics, Department of Neurology and.
  • Wahnich A; Program in Neurogenetics, Department of Neurology and.
  • Gao F; Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA.
  • Becherel OJ; Radiation Biology and Oncology Laboratory, University of Queensland, UQ Centre for Clinical Research, Herston, Australia.
  • Wang X; Program in Neurogenetics, Department of Neurology and.
  • Fike F; Department of Pathology and Laboratory Medicine and.
  • Chen L; Program in Neurogenetics, Department of Neurology and.
  • Criscuolo C; Department of Neuroscience and Reproductive and Odontostomatological Sciences, Federico II University, Napoli, Italy.
  • De Michele G; Department of Neuroscience and Reproductive and Odontostomatological Sciences, Federico II University, Napoli, Italy.
  • Filla A; Department of Neuroscience and Reproductive and Odontostomatological Sciences, Federico II University, Napoli, Italy.
  • Collins A; Department of Pediatrics and Department of Neurology, Children's Hospital Colorado, University of Colorado, Denver, School of Medicine, Aurora, CO, USA.
  • Hahn AF; Department of Clinical Neurological Sciences, Western University, London, Ontario, Canada and.
  • Gatti RA; Department of Pathology and Laboratory Medicine and Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Konopka G; Department of Neuroscience, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, USA.
  • Perlman S; Program in Neurogenetics, Department of Neurology and.
  • Lavin MF; Radiation Biology and Oncology Laboratory, University of Queensland, UQ Centre for Clinical Research, Herston, Australia.
  • Geschwind DH; Program in Neurogenetics, Department of Neurology and Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Coppola G; Program in Neurogenetics, Department of Neurology and Department of Psychiatry, Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA.
Hum Mol Genet ; 23(18): 4758-69, 2014 Sep 15.
Article en En | MEDLINE | ID: mdl-24760770
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ataxia / ADN Helicasas / ARN Helicasas / Redes Reguladoras de Genes / Síndrome de Cogan / Esclerosis Amiotrófica Lateral Límite: Animals / Humans Idioma: En Año: 2014 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ataxia / ADN Helicasas / ARN Helicasas / Redes Reguladoras de Genes / Síndrome de Cogan / Esclerosis Amiotrófica Lateral Límite: Animals / Humans Idioma: En Año: 2014 Tipo del documento: Article