Abnormal behaviours relevant to neurodevelopmental disorders in Kirrel3-knockout mice

In the nervous system, Kirrel3 is involved in neuronal migration, axonal fasciculation, and synapse formation. Recently, genetic links have been reported between mutations in the KIRREL3 gene and increased risk of neurodevelopmental disorders, including autism spectrum disorder (ASD) and intellectua...

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Detalles Bibliográficos
Autores principales: Hisaoka, Tomoko, Komori, Tadasuke, Kitamura, Toshio, Morikawa, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780462/
https://www.ncbi.nlm.nih.gov/pubmed/29362445
http://dx.doi.org/10.1038/s41598-018-19844-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780462/
https://www.ncbi.nlm.nih.gov/pubmed/29362445
http://dx.doi.org/10.1038/s41598-018-19844-7

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