1. De Franco, Elisa, Saint-Martin, Cécile, Brusgaard, Klaus, Bellanné-Chantelot, Christine, Flanagan, Sarah E. 2020. Update of variants identified in the pancreatic β-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes. In Human mutation, 41, 884-905. doi:10.1002/humu.23995. https://pubmed.ncbi.nlm.nih.gov/32027066/
2. Qin, Chenxi, Diaz-Gallo, Lina-Marcela, Tang, Bowen, Askling, Johan, Hägg, Sara. 2023. Repurposing antidiabetic drugs for rheumatoid arthritis: results from a two-sample Mendelian randomization study. In European journal of epidemiology, 38, 809-819. doi:10.1007/s10654-023-01000-9. https://pubmed.ncbi.nlm.nih.gov/37052755/
3. Azimi, Melika, Paseban, Melika, Ghareh, Sahar, Bandarian, Fatemeh, Hasanzad, Mandana. 2023. Association of ABCC8 gene variants with response to sulfonylurea in type 2 diabetes mellitus. In Journal of diabetes and metabolic disorders, 22, 649-655. doi:10.1007/s40200-023-01189-2. https://pubmed.ncbi.nlm.nih.gov/37255830/
4. Kapoor, Ritika R, Flanagan, Sarah E, Arya, Ved Bhushan, Ellard, Sian, Hussain, Khalid. 2013. Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. In European journal of endocrinology, 168, 557-64. doi:10.1530/EJE-12-0673. https://pubmed.ncbi.nlm.nih.gov/23345197/
5. Haghvirdizadeh, Polin, Sadat Haerian, Monir, Haghvirdizadeh, Pantea, Sadat Haerian, Batoul. 2014. ABCC8 genetic variants and risk of diabetes mellitus. In Gene, 545, 198-204. doi:10.1016/j.gene.2014.04.040. https://pubmed.ncbi.nlm.nih.gov/24768178/
6. Li, Meng, Han, Xueyao, Ji, Linong. 2021. Clinical and Genetic Characteristics of ABCC8 Nonneonatal Diabetes Mellitus: A Systematic Review. In Journal of diabetes research, 2021, 9479268. doi:10.1155/2021/9479268. https://pubmed.ncbi.nlm.nih.gov/34631896/
智鼠故事 
