Ruling in a suspect: the role of AP2S1 mutations in familial hypocalciuric hypercalcemia type 3

J Clin Endocrinol Metab. 2013 Dec;98(12):4666-9. doi: 10.1210/jc.2013-3616.
No abstract available

Publication types

  • Editorial
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Adaptor Protein Complex 2 / genetics*
  • Adaptor Protein Complex sigma Subunits / genetics*
  • Calcium, Dietary*
  • Contraindications
  • Female
  • Humans
  • Hypercalcemia / diet therapy
  • Hypercalcemia / genetics
  • Hypercalcemia / prevention & control*
  • Mutation*

Substances

  • AP2S1 protein, human
  • Adaptor Protein Complex 2
  • Adaptor Protein Complex sigma Subunits
  • Calcium, Dietary

Supplementary concepts

  • Familial benign hypercalcemia, type 3