Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea-Reference-Cited by-同舟云学术

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Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea

Published:2017 Issue:3 Volume:58 Page:527
ISSN:0513-5796
Container-title:Yonsei Medical Journal
language:en
Short-container-title:Yonsei Med J

Author:

Choi Jin-Ho¹,Jung Chang-Woo¹,Kang Eungu¹,Kim Yoon-Myung¹,Heo Sun Hee²,Lee Beom Hee¹,Kim Gu-Hwan³,Yoo Han-Wook¹

Affiliation:

1. Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

2. Asan Institute for Life Sciences, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

3. Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

Funder

National Research Foundation of Korea

Publisher

Yonsei University College of Medicine

Subject

General Medicine

Link

https://synapse.koreamed.org/pdf/10.3349/ymj.2017.58.3.527

Cited by 8 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. Toward clinical exomes in diagnostics and management of male infertility;The American Journal of Human Genetics;2024-05

2. Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report;World Journal of Clinical Cases;2022-11-06

3. Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years;eClinicalMedicine;2022-09

4. Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients;Frontiers in Endocrinology;2021-09-13

5. Genetic Anomalies of Growth Hormone Deficiency in Pediatrics;Endocrine, Metabolic & Immune Disorders - Drug Targets;2021-02-12

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