Accumulated common variants in the broader fragile X gene family modulate 
autistic phenotypes

Stepniak, Beata; Kästner, Anne; Poggi, Giulia; Mitjans, Marina; Begemann, Martin; Hartmann, Annette; Van der Auwera, Sandra; Sananbenesi, Farahnaz; Krueger-Burg, Dilja; Matuszko, Gabriela; Brosi, Cornelia; Homuth, Georg; Völzke, Henry; Benseler, Fritz; Bagni, Claudia; Fischer, Utz; Dityatev, Alexander; Grabe, Hans-Jörgen; Rujescu, Dan; Fischer, Andre; Ehrenreich, Hannelore

doi:10.15252/emmm.201505696

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Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes

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Stepniak, Beata
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182235

Kästner, Anne
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182353

Poggi, Giulia
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182304

Mitjans, Marina
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182563

Begemann, Martin
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182261

Krueger-Burg, Dilja
Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182084

Benseler, Fritz
Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons182138

Ehrenreich, Hannelore
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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Stepniak, B., Kästner, A., Poggi, G., Mitjans, M., Begemann, M., Hartmann, A., et al. (2015). Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. EMBO molecular medicine, 7(12), 1565-1579. doi:10.15252/emmm.201505696.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0029-7393-0

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