A novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III - Monticone, S; Hattangady, N G; Penton, D; Isales, C; Edwards, M A; Williams, T A; Sterner, C; Warth, R; Mulatero, P; Rainey, W E (J Clin Endocrinol Metab, 2013)