A Novel <i>TBX19</i> Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.

Akcan, Nese; Serakinci, Nedime; Turkgenc, Burcu; Bundak, Ruveyde; Bahceciler, Nerin; Temel, Sehime G

A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.

Akcan, Nese; Serakinci, Nedime; Turkgenc, Burcu; Bundak, Ruveyde; Bahceciler, Nerin; Temel, Sehime G.

Affiliation

Akcan N; Faculty of Medicine, Department of Pediatric Endocrinology, University of Near East, Nicosia, Cyprus.
Serakinci N; Faculty of Medicine, Department of Medical Genetics, University of Near East, Nicosia, Cyprus.
Turkgenc B; Genetic Diagnostic Center, University of Acibadem, Istanbul, Turkey.
Bundak R; Faculty of Medicine, Department of Pediatric Endocrinology, University of Kyrenia, Kyrenia, Cyprus.
Bahceciler N; Faculty of Medicine, Department of Pediatric Allergy and Immunology, University of Near East, Nicosia, Cyprus.
Temel SG; Faculty of Medicine, Department of Histology and Embryology, University of Near East, Nicosia, Cyprus.

Front Endocrinol (Lausanne) ; 8: 64, 2017.

Article in En | MEDLINE | ID: mdl-28458651