CELF4

Publications

Barone R et al. Familial 18q12.2 deletion supports the role of RNAbinding protein CELF4 in autism spectrum disorders. Am J Med Genet Part A. 2017;,173(6):1649–1655. PMID: 28407444.

Gilling M et al. (2008). A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. Eur J Hum Genet. 2008;16(3): 312–319. PMID: 18183041.

Halgren C et al. Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity. Eur J Hum Genet. 2012;20(12):1315–1319. PMID: 22617346.