Partial GCK gene deletion mutations causing maturity-onset diabetes of the young-Reference-Cited by-同舟云学术

Partial GCK gene deletion mutations causing maturity-onset diabetes of the young

Published:2023-09-13 Issue:1 Volume:61 Page:107-115
ISSN:1432-5233
Container-title:Acta Diabetologica
language:en
Short-container-title:Acta Diabetol

Author:

Yu Ruiqi,Zhang Haichen,Xiao Xinhua^ORCID

Funder

Natural Science Foundation of Beijing Municipality

Beijing Municipal Science and Technology Commission

National High Level Hospital Clinical Research Funding

Key Technologies Research and Development Program

CAMS Innovation Fund for Medical Sciences

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00592-023-02173-1.pdf

Reference26 articles.

1. Ellard S, Thomas K, Edghill EL et al (2007) Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young. Diabetologia 50(11):2313–2317. https://doi.org/10.1007/s00125-007-0798-6

2. Wang X, Lam SM, Cao M et al (2021) Localized increases in CEPT1 and ATGL elevate plasmalogen phosphatidylcholines in HDLs contributing to atheroprotective lipid profiles in hyperglycemic GCK-MODY. Redox Biol 40:101855. https://doi.org/10.1016/j.redox.2021.101855

3. Berberich AJ, Huot C, Cao H et al (2019) Copy number variation in GCK in patients with maturity-onset diabetes of the young. J Clin Endocrinol Metab 104(8):3428–3436. https://doi.org/10.1210/jc.2018-02574

4. Zhang B, Feng Z, Zhang L (1998) A study on the physical development of newborns of different gestational ages in 15 cities in China. Chin J Pediatr 26(4):206–208

5. Wang K, Li M, Hakonarson H (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38(16):e164–e164. https://doi.org/10.1093/nar/gkq603