LDLR and familial hyperaldosteronism: In addition, this allelic variant in compoundheterozygosity with EX7_EX10del (c.941-?_1186+?del) inthe LDLR gene has been reported in Brazil, and together withc.55G>C (p.Asp19His) within the ABCG8 gene in FH patientsin Malaysia (Jannes et al., 2015; Mohd Nor et al., 2019).