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