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A Role for the Chromatin-Remodeling Factor BAZ1A in Neurodevelopment.
Zaghlool, Ammar; Halvardson, Jonatan; Zhao, Jin J; Etemadikhah, Mitra; Kalushkova, Antonia; Konska, Katarzyna; Jernberg-Wiklund, Helena; Thuresson, Ann-Charlotte; Feuk, Lars.
Afiliación
  • Zaghlool A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Halvardson J; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Zhao JJ; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Etemadikhah M; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Kalushkova A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Konska K; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Jernberg-Wiklund H; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Thuresson AC; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
  • Feuk L; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Sweden.
Hum Mutat ; 37(9): 964-75, 2016 09.
Article en En | MEDLINE | ID: mdl-27328812

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Discapacidad Intelectual / Sistema Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Discapacidad Intelectual / Sistema Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Suecia
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