A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy-Reference-Cited by-同舟云学术

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A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy

Published:2012-01-01 Issue:1-2 Volume:25 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Hung Ching-Ngar,Poon Wing-Tat,Lee Ching-Yin,Law Chun-Yiu,Chan Albert Yan-Wo

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/jpem-2011-0437/pdf

Cited by 18 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. Medical semiology of patients with monogenic obesity: A systematic review;Obesity Reviews;2024-07-02

2. Body Fat Distribution Contributes to Defining the Relationship between Insulin Resistance and Obesity in Human Diseases;Current Diabetes Reviews;2023-08-16

3. Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use;Genetics in Medicine;2023-07

4. Gene expression atlas of energy balance brain regions;JCI Insight;2021-08-23

5. Two Cases With an Early Presented Proopiomelanocortin Deficiency—A Long-Term Follow-Up and Systematic Literature Review;Frontiers in Endocrinology;2021-06-09

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