Associated Papers
Establishing a Mouse Model of NL3R617W-Associated Autism Spectrum Disorder for a Functional Study.
Gao W et al.
Actas Espanolas De Psiquiatria, 2025
Analyses of Human Genetic Data to Identify Clinically Relevant Domains of Neuroligins.
Lehr AW et al.
Genes, 2024
Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics.
Nguyen TA et al.
Frontiers in Synaptic Neuroscience, 2020
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.
Quartier A et al.
Human Mutation, 2019
Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.
Xu X et al.
Brain and Behavior, 2017
Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort.
Landini M et al.
International Journal of Molecular Sciences, 2016
Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
Xu X et al.
Molecular Biology Reports, 2014
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