MODY in China: Two Families Carrying the KCNJ11 E229K Variant
Overview
Overview
Authors
Authors
Affiliations
Affiliations
Soon will be listed here.
References
1.
He B, Li X, Zhou Z
. Continuous spectrum of glucose dysmetabolism due to the KCNJ11 gene mutation-Case reports and review of the literature. J Diabetes. 2020; 13(1):19-32.
DOI: 10.1111/1753-0407.13114.
View
2.
Liu L, Nagashima K, Yasuda T, Liu Y, Hu H, He G
. Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes. Diabetologia. 2013; 56(12):2609-18.
PMC: 5333983.
DOI: 10.1007/s00125-013-3031-9.
View
3.
Bonfanti R, Iafusco D, Rabbone I, Diedenhofen G, Bizzarri C, Patera P
. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy. Eur J Endocrinol. 2021; 184(4):575-585.
DOI: 10.1530/EJE-20-1030.
View
4.
Babiker T, Vedovato N, Patel K, Thomas N, Finn R, Mannikko R
. Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes. Diabetologia. 2016; 59(6):1162-6.
PMC: 4869695.
DOI: 10.1007/s00125-016-3921-8.
View