A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin oleh Théo Charnay, Théo Charnay, Gregory Mougel, Gregory Mougel, Cyril Amouroux, Iva Gueorguieva, Florence Joubert, Morgane Pertuit, Rachel Reynaud, Rachel Reynaud, Anne Barlier, Anne Barlier, Thierry Brue, Thierry Brue, Alexandru Saveanu, Alexandru Saveanu