CYP24A1 mutations in idiopathic infantile hypercalcemia

N Engl J Med. 2011 Nov 3;365(18):1741-2; author reply 1742-3. doi: 10.1056/NEJMc1110226.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Animals
  • Female
  • Humans
  • Hypercalcemia / genetics*
  • Male
  • Mutation*
  • Steroid Hydroxylases / genetics*
  • Vitamin D / adverse effects*

Substances

  • Vitamin D
  • Steroid Hydroxylases