copy number variation risk_factor_for autism spectrum disorder

Subject: copy number variation
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

genome-wide studies of CNV in ... Autism Spectrum Disorders (ASDs)

confidence: 0.95