| Literature DB >> 25910996 |
Abstract
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)
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Year: 2015 PMID: 25910996 DOI: 10.1016/j.ando.2015.03.013
Source DB: PubMed Journal: Ann Endocrinol (Paris) ISSN: 0003-4266 Impact factor: 2.478