A novel PROP1 gene mutation (157delA) in Japanese siblings with combined anterior pituitary hormone deficiency
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2004.02147.x/fullpdf
Reference42 articles.
1. Adrenocorticotropin Deficiency in Combined Pituitary Hormone Deficiency Patients Homozygous for a Novel PROP1 Deletion
2. A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty
3. Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene
4. 1 Aetiology and pathogenesis of growth hormone deficiency
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1. Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome;Frontiers in Pediatrics;2021-02-02
2. Congenital Hypopituitarism: Various Genes, Various Phenotypes;Hormone and Metabolic Research;2019-02
3. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery;Archives of Endocrinology and Metabolism;2019
4. Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes;Journal of Human Genetics;2017-03-30
5. Combined Pituitary Hormone Deficiency;Growth Hormone Deficiency;2016
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