Kristi Niblo

No ORCID on file · 1 paper in corpus · active 2018
2018
Disruption of the KH1 domain of Fmr1 leads to transcriptional alterations and attentional deficits in rats
·doi:10.1101/338988

Fragile X Syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the FMR1 gene. FXS is a leading monogenic cause of autism spectrum disorder (ASD) and inherited intellectual disability (ID). In most cases, the mutation is a…