LDLR and familial hyperaldosteronism: We identified 14 mutations in the LDL receptor gene that are probably causative for FH development, namely, c.192del10/ins8, c.195–196insT, p. (Ser206Arg), c.925–931del7, p. (Ser447Cys), p. (Leu511Ser), c.1686del8/insT, p. (Leu646Ile), c.2191delG, c.313+2T>G, p. (Cys82Ser), p. (Glu408Lys), p. (Trp443Arg), and p. (Trp620Ser).