Combined Pituitary Hormone Deficiency Caused by a Novel Mutation of a Highly Conserved Residue (F88S) in the Homeodomain of PROP-1
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 48 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. DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues;Nature Communications;2024-04-10
3. Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins;Hormones;2023-12-26
4. GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature;Frontiers in Endocrinology;2020-08-28
5. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery;Archives of Endocrinology and Metabolism;2019
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