NLGN4X risk_factor_for autism spectrum disorder

Subject: NLGN4X
Relation: risk_factor_for
Object: autism spectrum disorder
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited

These genes include NLGN4X ... recognized as bona fide risk factors for ASDs.

confidence: 0.96