Associated Papers
Exploring the Landscape of Pre- and Post-Synaptic Pediatric Disorders with Epilepsy: A Narrative Review on Molecular Mechanisms Involved.
Scorrano G et al.
International Journal of Molecular Sciences, 2024
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.
Quartier A et al.
Human Mutation, 2019
Metastatic tumor evolution and organoid modeling implicate TGFBR2 as a cancer driver in diffuse gastric cancer.
Nadauld LD et al.
Genome Biology, 2014
25315765 (PubMed )
Supplement: 13059_2014_428_MOESM1_ESM.pdf
Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.
Yanagi K et al.
Autism Research and Treatment, 2012
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.
Yu J et al.
Behavioral and Brain Functions : Bbf, 2011
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