A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and sever... by Hannan, F, Nesbit, M, Christie, P, Lissens, W, Van der Schueren, B, Bex, M, Bouillon, R, Thakker, R

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. by Yao, L, Schiavi, F, Cascon, A, Qin, Y, Inglada-Pérez, L, King, E, Toledo, R, Ercolino, T, Rapizzi, E, Ricketts, C, Mori, L, Giacchè, M, Mendola, A, Taschin, E, Boaretto, F, Loli, P, Iacobone, M, Rossi, G, Biondi, B, Lima-Junior, J, Kater, C, Bex, M, Vikkula, M, Grossman, AB, Gruber, S