Associated Papers
Prevalence and Clinical Characteristics of NEUROD1-MODY in Chinese Early-Onset Type 2 Diabetes Mellitus and a Literature Review.
Ba T et al.
Journal of Diabetes, 2025
40148250 (PubMed )
Supplement: JDB-17-e70080-s001.docx
Maturity-Onset Diabetes of the Young: Mutations, Physiological Consequences, and Treatment Options.
Younis H et al.
Journal of Personalized Medicine, 2022
A Functional Variant Rs492554 Associated With Congenital Heart Defects Modulates SESN2 Expression Through POU2F1.
Yang W et al.
Frontiers in Cell and Developmental Biology, 2021
34249922 (PubMed )
Supplement: Table_1.xls › D1D2D3
Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis.
Liu YX et al.
Frontiers in Pediatrics, 2021
[Contribution of MODY6 gene in the pathogenesis of familial type 2 diabetes in Chinese population].
Han XY et al.
Zhonghua Yi Xue Za Zhi, 2005
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