CEP152 and microcephaly: Chen et al., 2017) whose mutations in patients cause microcephaly (Care4Rare Canada Consortium et al., 2015; Grandone et al., 2016), dwarfism, and polymicrogyria (Kheradmand Kia et al., 2012) (Figure 4a; Supplementary file 1). Stable HEK293T T-REX Flp-In cell lines showed normal centriolar localization as determined via confocal imaging with the marker CEP152 (Figure 5f).