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16p11.2 deletion associated_with epilepsy

Subject
16p11.2 deletion
Relation
associated_with
Object
epilepsy
p-value
Evidence from: primary | all sources

Evidence (1 sources)

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited
reciprocal rearrangements of 16p11.2 ... influence ... susceptibility to epilepsy
confidence: 0.90