EML1

Publications

Kielar M et al. Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. Nat Neurosci. 2014;17(7):923–933. PMID: 24859200.

Markus F et al. A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects. J Hum Genet. 2021;66(12):1159-1167. PMID: 34211111.

Nagaraj UD et al. Prenatal and postnatal evaluation of polymicrogyria with band heterotopia. Radiol Case Rep. 2017;12(3):602–605. PMID: 28828134.

Oegema R et al. EML1-associated brain overgrowth syndrome with ribbon-like heterotopia. Am J Med Genet C Semin Med Genet 2019;181(4):627-637. PMID: 31710781.

Shaheen R et al. The genetic landscape of familial congenital hydrocephalus. Annals of Neurology. 2017; 81(6):890–897. PMID: 28556411.