A novel Founder Mutation of CYP21A2 in Patients with CAH due to 21-Hydroxylase Deficiency

TORAMAN B., KARAGÜZEL G., KALAY E., DİNÇER T.

ESPE DUBLIN, Dublin, Ireland, 20 - 22 September 2014, pp.1-7

  • Publication Type: Conference Paper / Full Text
  • City: Dublin
  • Country: Ireland
  • Page Numbers: pp.1-7
  • Karadeniz Technical University Affiliated: Yes