ARID2

Publications

Bramswig N C et al. Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype. Hum Genet. 2017;136(3):297-305.  PMID: 28124119.

Gazdagh G et al. Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients. Eur J Med Genet. 2018.  PMID: 29698805.

Schrier Vergano S et al. Coffin-Siris Syndrome. In Pagon R A et al. (Eds.). GeneReviews(R). Seattle (WA). 1993.  PMID: 23556151.

Shang L et al. Mutations in ARID2 are associated with intellectual disabilities. Neurogenetics. 2015;16(4):307-314.  PMID: 26238514.

Van Paemel R et al. Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability. Am J Med Genet A. 2017;173(11):3104-3108.  PMID: 28884947.