A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections
Author:
Publisher
Frontiers Media SA
Subject
Endocrinology, Diabetes and Metabolism
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1. A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin;Frontiers in Endocrinology;2023-02-15
2. A serious and unusual presentation of congenital isolated ACTH deficiency due to TBX19 mutation, beyond the neonatal period;Endocrinology, Diabetes & Metabolism Case Reports;2022-09-01
3. Insights into non-classic and emerging causes of hypopituitarism;Nature Reviews Endocrinology;2020-11-27
4. Headliner in Physiology and Management of Childhood Asthma: Hypothalamic-Pituitary-Adrenal Axis;Current Pediatric Reviews;2020-04-09
5. Development of the Pituitary Gland;Comprehensive Physiology;2020-03-12
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