A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 79 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Common and Uncommon Mouse Models of Growth Hormone Deficiency;Endocrine Reviews;2024-06-10
2. Hypoprolactinemia. Does it matter? Redefining the hypopituitarism and return from a mumpsimus;Reviews in Endocrine and Metabolic Disorders;2023-10-25
3. POU1F1/Pou1f1 c.143-83A > G Variant Disrupts the Branch Site in Pre-mRNA and Leads to Dwarfism;Endocrinology;2022-11-26
4. A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees;Genes;2022-04-08
5. POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature;Pituitary;2021-03-20
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