A novel founder mutation of CYP21A2 in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

KARAGÜZEL G.

Annual Meeting for the European Society for Pediatric Endocrinology, 18th-20th September, 2014, Dublin, Ireland, 18 - 20 September 2014, pp.3

  • Publication Type: Conference Paper / Full Text
  • City: Dublin
  • Country: Ireland
  • Page Numbers: pp.3
  • Karadeniz Technical University Affiliated: Yes