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Paper Details

Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability.
PLoS One
3
2021
CRE, CRE variants, FMR1CRE, FMRP, Fmr1, Fmr1CRE, Mouse, TENM1CRE, X chromosome, X-linked intellectual disability, XLID, chrX CRE, cis-regulatory elements, cis-regulatory variants, coding regions, mice, neurodevelopmental disorders, ultra-rare CRE variant, zebrafish
Author NameAffiliation
Detelina GrozevaCambridge Institute for Medical Research, University of Cambridge
Detelina GrozevaInstitute of Psychological Medicine & Clinical Neurosciences, Cardiff University
James G D PrendergastRoslin Institute, University of Edinburgh
Graeme R GrimesInstitute of Genomic and Molecular Medicine, University of Edinburgh
Olivera Spasic-BoskovicAdden brooke's Hospital, Cambridge University Hospitals NHS Foundation Trust Cambridge
Frances Lucy RaymondCambridge Institute for Medical Research, University of Cambridge
David R FitzPatrickUniversity of Edinburgh (UoE)
David R FitzPatrickUniversity of Edinburgh
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