Article
Identification of FMRP target genes expressed in corticogenesis: implication for common phenotypes among neurodevelopmental disorders
2019-09-18
Abstract excerpt
<h4>ABSTRACT</h4> Fragile X mental retardation protein (FMRP) is encoded by FMR1 gene that is responsible for Fragile X Syndrome (FXS) showing intellectual disability and autism spectrum disorder. FMRP is an RNA binding protein highly expressed in the brain. Although several target genes for FMRP have been identified, limited studies have suggested the role of FMRP in corticogenesis. Here we performed RNA immuno...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- c5fc95cf-1452-5fcb-803b-b27cc12a001a
- DOI
- 10.1101/769026
