RBMX and syndromic intellectual disability: The double role of RBMX in genome maintenance via both direct participation in the DNA damage response and splicing regulation of genome stability genes could explain why mutations of RBMX are associated with an intellectual disability syndrome (Cai et al., 2021; Shashi et al., 2015), and why RBMX has been identified as a potential tumour suppressor (Adamson et al., 2012; Elliott et al., 2019).