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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...
Uloženo v:
| Vydáno v: | Sci Rep |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5780462/ https://ncbi.nlm.nih.gov/pubmed/29362445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-19844-7 |
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