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Article

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism.

Psychiatric genetics - 1 Oct 2013

Volaki Konstantina, Pampanos Andreas, Kitsiou-Tzeli Sophia, Vrettou Christina, Oikonomakis Vasilis, Sofocleous Christalena, Kanavakis Emmanuel

Abstract excerpt

Molecular and neurobiological evidence for the involvement of neuroligins (particularly NLGN3 and NLGN4X genes) in autistic disorder is accumulating. However, previous mutation screening studies on these two genes have yielded controversial results. The present study explores, for the first time, the contribution of NLGN3 and NLGN4X genetic variants in Greek patients with autistic disorder. We analyzed the full...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23851596
DOI: 10.1097/YPG.0b013e3283643644

Genes

NLGN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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