LDLR and familial hyperaldosteronism: The most commonly observed mutations in LDLR were c.301G > A (p.(Glu101Lys)) present in six probands, c.259T > G (p.(Trp87Gly)), c.313+1G > A, c.680_681delAC (p.(Asp227Glyfs*12)), c.681C > G (p.(Asp227Glu)), c.1116_1119dupGGGT (p.(Glu374fs*8)), and c.2054C > T (p.(Pro685Leu)), all observed in three FH probands.