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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465329/ https://www.ncbi.nlm.nih.gov/pubmed/32873342 http://dx.doi.org/10.1186/s13229-020-00373-y |