A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds - Groussin, L; Horvath, A; Jullian, E; Boikos, S; Rene-Corail, F; Lefebvre, H; Cephise-Velayoudom, F L; Vantyghem, M C; Chanson, P; Conte-Devolx, B; Lucas, M; Gentil, A; Malchoff, C D; Tissier, F; Carney, J A; Bertagna, X; Stratakis, C A; Bertherat, J (J Clin Endocrinol Metab, 2006)