Publication | Open Access

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

Unexplained Intellectual DisabilityGender-specific EffectsMendelian DisorderGenetic DisorderGeneticsFragile X SpectrumGenetic FactorNeuroscienceDisease Gene IdentificationMedicineCommon CauseNeurogeneticsDevelopmental Delay