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Autism-associated variants of neuroligin 4X impair synaptogenic activity by various molecular mechanisms
BACKGROUND: Several genetic alterations, including point mutations and copy number variations in NLGN genes, have been associated with psychiatric disorders, such as autism spectrum disorder (ASD) and X-linked mental retardation (XLMR). NLGN genes encode neuroligin (NL) proteins, which are adhesion...
Zapisane w:
| Wydane w: | Mol Autism |
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| Główni autorzy: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BioMed Central
2020
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7465329/ https://ncbi.nlm.nih.gov/pubmed/32873342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-020-00373-y |
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