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Entries: 1-3  
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Complexin2 null mutation requires a ‘second hit’ for induction of phenotypic changes relevant to schizophrenia.
Authors: Radyushkin, K.; El-Kordi, A.; Boretius, S.; Castaneda, S.; Ronnenberg, A.; Reim, K.; Bickeboeller, H.; Frahm, J.; Brose, N.; Ehrenreich, H.
Date of Publication (YYYY-MM-DD): 2010-08
Title of Journal: Genes, Brain and Behavior
Volume: 9
Issue / Number: 6
Start Page: 592
End Page: 602
Document Type: Article
ID: 493923.0
Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.
Authors: Radyushkin, K.; Hammerschmidt, K.; Boretius, S.; Varoqueaux, F.; El-Kordi, A.; Ronnenberg, A.; Winter, D.; Frahm, J.; Fischer, J.; Brose, N.
Date of Publication (YYYY-MM-DD): 2009-06
Title of Journal: Genes, Brain and Behavior
Volume: 8
Issue / Number: 4
Start Page: 416
End Page: 425
Document Type: Article
ID: 430731.0
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.
Authors: Jamain, S.; Radyushkin, K.; Hammerschmidt, K.; Granon, S.; Boretius, S.; Varoqueaux, F.; Ramanantsoa, N.; Gallego, J.; Ronnenberg, A.; Winter, D.; Frahm, J.; Fischer, J.; Bourgeron, T.; Ehrenreich, H.; Brose, N.
Date of Publication (YYYY-MM-DD): 2008-01-28
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 105
Issue / Number: 5
Start Page: 1710
End Page: 1715
Document Type: Article
ID: 337218.0
Entries: 1-3  
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