Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency-Reference-Cited by-同舟云学术

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Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency

Published:2024-05 Issue: Volume:907 Page:148283
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Wei Shuoshuo,Zhang Mei,Li Yanying,Yang Wanling,Zhang Chuanpeng,Liu Fupeng^ORCID,Chen Shuxiong,Ban Bo,He Dongye^ORCID

Funder

Jining Medical University

National Key Clinical Specialty Discipline Construction Program of China

Publisher

Elsevier BV

Reference34 articles.

1. Genetic causes and treatment of isolated growth hormone deficiency-an update;Alatzoglou;Nat. Rev. Endocrinol.,2010

2. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency;Alatzoglou;J. Clin. Endocr. Metab.,2009

3. Isolated growth hormone deficiency (GHD) in childhood and adolescence: recent advances;Alatzoglou;Endocr. Rev.,2014

4. A mouse with targeted ablation of the growth hormone-releasing hormone gene: a new model of isolated growth hormone deficiency;Alba;Endocrinol.,2004

5. Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: frequencies, phenotypes and growth outcomes;Blum;EBioMedicine.,2018

Cited by 1 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

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