PCSK9 and familial hyperaldosteronism: The p.Asp90Gly mutation in LDLR was reported in phenotypic FH patients from Western Australia who were screened for LDLR, APOB and PCSK9 mutations (Hooper et al., 2012), while p.Glu31Lys has been reported in Asian Indian FH patients (Setia et al., 2020) and p.Phe282Leu was observed in Czech probands suspected to have FH (Tichý et al., 2012).