Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3
Author:
Publisher
BMJ
Subject
Genetics(clinical),Genetics
Cited by 72 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. Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes;Journal of Diabetes Investigation;2024-07-06
2. Natural history of Wolcott‐Rallison syndrome: A systematic review and follow‐up study;Liver International;2024-01-17
3. Wolcott-Rallison Syndrome, a Rare Cause of Permanent Diabetes Mellitus in Infants—Case Report;Pediatric Reports;2023-10-16
4. The missing link between genetic association and regulatory function;eLife;2022-12-14
5. Exocrine-Endocrine Crosstalk: The Influence of Pancreatic Cellular Communications on Organ Growth, Function and Disease;Frontiers in Endocrinology;2022-06-13
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