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de novo variant associated_with familial cases

Subject
de novo variant
Relation
associated_with
Object
familial cases
p-value
Evidence from: primary | all sources

Evidence (1 sources)

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited
high rate in sporadic cases (10%) as compared with “familial” cases and controls.
confidence: 0.80