MeCP2 associated_with Rett syndrome

Subject: MeCP2
Relation: associated_with
Object: Rett syndrome
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

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

mutations in the Rett Syndrome gene MeCP2

confidence: 0.97