CYP21A2 gene mutation in South Indian children with congenital adrenal hyperplasia

Indian Pediatr. 2015 Aug;52(8):710-1.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adrenal Hyperplasia, Congenital / genetics*
  • DNA Mutational Analysis
  • Female
  • Humans
  • India
  • Infant
  • Infant, Newborn
  • Male
  • Mutation / genetics*
  • Steroid 21-Hydroxylase / genetics*

Substances

  • CYP21A2 protein, human
  • Steroid 21-Hydroxylase