Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Original publication

DOI

10.1016/j.ando.2015.03.013

Type

Journal article

Journal

Ann Endocrinol (Paris)

Publication Date

05/2015

Volume

76

Pages

81 - 83

Keywords

AP2σ, Autosomal dominant hypocalcaemia, Calcium-sensing receptor (CaSR), Familial (benign) hypocalciuric hypercalcaemia, GNA11, Gain-of-function mutations, Hypercalcémie bénigne familiale hypocalciurique, Hyperparathyroïdie primaire, Hypocalcémie autosomique dominante, Loss-of-function mutations, Mutation perte-de-fonction, Mutations gain-de-fonction, Primary hyperparathyroidism, Récepteur sensible au calcium (CaSR), Animals, Humans, Hypocalcemia, Parathyroid Diseases, Parathyroid Glands, Receptors, Calcium-Sensing, Receptors, G-Protein-Coupled