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.
Authors
Elizabeth A Streeten
,
Kiarash Zarbalian
,
Coleen M Damcott
PMID:
22047572
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
Grants and funding
P30 DK072488/DK/NIDDK NIH HHS/United States