familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del


BİDECİ A. , DÖĞER E. , DEMET AKBAŞ E., KILINÇ UĞURLU A., GÜRAN T., ÇAMURDAN M. O. , ...More

10. international meeting of pediatric endocrinology, Washington, Kiribati, 14 - 17 September 2017

  • Publication Type: Conference Paper / Summary Text
  • City: Washington
  • Country: Kiribati