Associated Papers
Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances.
Zhang Y et al.
Journal of Integrative Neuroscience, 2024
Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions.
Feichtinger RG et al.
Genes, 2023
NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES results.
Kamal N et al.
Gene, 2023
Advances in neurexin studies and the emerging role of neurexin-2 in autism spectrum disorder.
Khoja S et al.
Frontiers in Molecular Neuroscience, 2023
36923655 (PubMed )
Supplement: Table_1.XLSX › NRXN3
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