Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants. - Jacobs EZ; Brown K; Byler MC; D'haenens E; Dheedene A; Henderson LB; Humberson JB; van Jaarsveld RH; Kanani F; Lebel RR; Millan F; Oegema R; et al. (Clinical genetics, 2021)