CEP63 and dyslexia: A number of other genes and types of variants such as copy number variations (Pagnamenta et al., 2010; Poelmans et al., 2009; Veerappa, Saldanha, Padakannaya, & Ramachandra, 2013) and rare coding mutations in CCDC136/FLNC, NCAN and CEP63 in isolated families (Adams et al., 2017; Einarsdottir et al., 2015, 2017) have been implicated in dyslexia.