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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...
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| Опубликовано в: : | Mol Autism |
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| Главные авторы: | , , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2020
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| Предметы: | |
| Online-ссылка: | 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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