Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications

Clin Endocrinol (Oxf). 2016 Sep;85(3):495-7. doi: 10.1111/cen.13104. Epub 2016 Jun 10.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Fractures, Bone / etiology*
  • Fractures, Bone / therapy
  • Humans
  • Hypocalcemia / genetics*
  • Hypocalcemia / therapy
  • Middle Aged
  • Mutation*
  • Pedigree
  • Receptors, Calcium-Sensing / genetics*

Substances

  • Receptors, Calcium-Sensing