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Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism

MPS-Authors
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El-Kordi,  Ahmed
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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Winkler,  Daniela
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/persons182261

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

/persons/resource/persons182377

Ronnenberg,  Anja
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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Ritter,  Caroline
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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Jatho,  Jasmin
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

/persons/resource/persons15679

Radyushkin,  Konstantin
Clinical neuroscience, Max Planck Institute of Experimental Medicine, Max Planck Society;

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Brose,  Nils
Molecular neurobiology, Max Planck Institute of Experimental Medicine, Max Planck Society;

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

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Citation

El-Kordi, A., Winkler, D., Hammerschmidt, K., Kästner, A., Krueger, D., Ronnenberg, A., et al. (2013). Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. Behavioural Brain Research, 251, 41-49. doi:10.1016/j.bbr.2012.11.016.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-510B-3
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