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, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• City: Washington
• Country: Kiribati
• Gazi University Affiliated: Yes