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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