Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay-Reference-Cited by-同舟云学术

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Familial Combined Pituitary Hormone Deficiency due to a Novel Mutation R99Q in the Hot Spot Region of Prophet of Pit-1 Presenting as Constitutional Growth Delay

Published:2003-01 Issue:1 Volume:88 Page:38-44
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Vieira Teresa C.,Dias da Silva Magnus R.,Cerutti Janete M.,Brunner Elisa,Borges Mariana,Arnaldi Liliane T.,Kopp Peter,Abucham Julio

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 42 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. DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues;Nature Communications;2024-04-10

2. 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

3. Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary;International Journal of Molecular Sciences;2019-04-16

4. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery;Archives of Endocrinology and Metabolism;2019

5. A Large PROP1 Gene Deletion in a Turkish Pedigree;Case Reports in Endocrinology;2018

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