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Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation.
Schwarz, Niklas; Uysal, Betül; Rosa, Filip; Löffler, Heidi; Mau-Holzmann, Ulrike A; Liebau, Stefan; Lerche, Holger.
Afiliación
  • Schwarz N; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany. Electronic address: niklas.schwarz@uni-tuebingen.de.
  • Uysal B; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany.
  • Rosa F; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany.
  • Löffler H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany.
  • Mau-Holzmann UA; Department of Medical Genetics and Applied Genomics, University of Tuebingen, Germany.
  • Liebau S; Institute of Neuroanatomy & Developmental Biology, University of Tuebingen, Germany.
  • Lerche H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany.
Stem Cell Res ; 37: 101445, 2019 05.
Article en En | MEDLINE | ID: mdl-31075689
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diferenciación Celular / Epilepsia / Canal de Potasio Kv.1.2 / Células Madre Pluripotentes Inducidas / Fibroblastos / Trastornos del Neurodesarrollo / Mutación Límite: Adult / Humans / Male Idioma: En Revista: Stem Cell Res Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diferenciación Celular / Epilepsia / Canal de Potasio Kv.1.2 / Células Madre Pluripotentes Inducidas / Fibroblastos / Trastornos del Neurodesarrollo / Mutación Límite: Adult / Humans / Male Idioma: En Revista: Stem Cell Res Año: 2019 Tipo del documento: Article