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Gorvin, CM, Hannan, FM ORCID: 0000-0002-2975-5170, Cranston, T, Valta, H, Makitie, O, Schalin-Jantti, C and Thakker, RV (2018) Cinacalcet rectifies hypercalcemia in a patient with familial hypocalciuric hypercalcemia type 2 (FHH2) caused by a germline loss-of-function Gα 11 mutation. Journal of Bone and Mineral Research, 31 (01). pp. 32-41.

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Piret, SE, Gorvin, CM, Pagnamenta, AT, Howles, SA, Cranston, T, Rust, N, Nesbit, MA, Glaser, B, Taylor, JC, Buchs, AE et al (show 2 more authors) , Hannan, F ORCID: 0000-0002-2975-5170 and Thakker, RV (2016) Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family with Autosomal Dominant Hypocalcemia Type 2 (ADH2). Journal of Bone and Mineral Research, 31 (6). pp. 1207-1214.