Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain.
- Cited forFUNCTION, INTERACTION WITH ARID4A, DISRUPTION PHENOTYPE
- CategoriesFunction, Interaction, Phenotypes & Variants
- SourceUniProtKB reviewed (Swiss-Prot)