Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.
<h4>Background</h4>Copy number variants have emerged as an important genomic cause of common, complex neurodevelopmental disorders. These usually change copy number of multiple genes, but deletions at 2p16.3, which have been associated with autism, schizophrenia and mental retardation, a...
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| Auteurs principaux: | , , , |
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| Format: | article |
| Langue: | EN |
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Public Library of Science (PLoS)
2013
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| Accès en ligne: | https://doaj.org/article/572a5183b1af4c6f8167db5aec08bb69 |
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