SLC13A5 citrate transporter disorder is a rare neurological disease caused by pathogenic loss-of-function variants in the SLC13A5 gene (Thevenon et al., 2014; Hardies et al., 2015; Klotz et al., 2016; Bainbridge et al., 2017; Matricardi et al., 2020; Yang et al., 2020). Here, SLC13A5 is linked to nervous system disorder.