Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism by Mannstadt, M, Nesbit, M, Howles, S, Rogers, A, Thakker, R, Jueppner, H

Hypoparathyroidism by Mannstadt, M, Bilezikian, JP, Thakker, RV, Hannan, FM, Clarke, BL, Rejnmark, L, Mitchell, DM, Vokes, TJ, Winer, KK, Shoback, DM

Knockin mouse with mutant Gα11 mimics human inherited hypocalcemia and is rescued by pharmacologic inhibitors by Roszko, K, Bi, R, Gorvin, C, Bräuner-Osborne, H, Xiong, X, Inoue, A, Thakker, R, Strømgaard, K, Gardella, T, Mannstadt, M

Hypoparathyroidism: genetics and diagnosis by Mannstadt, M, Cianferotti, L, Gafni, RI, Giusti, F, Kemp, EH, Koch, CA, Roszko, KL, Yao, L, Guyatt, GH, Thakker, RV, Xia, W, Brandi, M