MODY13 ist ein autosomal dominanter Typ 2 Diabetes, der sich aufgrund einer Mutation im KCNJ11-Gen entwickelt.
1. |
Yorifuji T et al. (2005) The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus. |
2. |
Prudente S et al. (2015) Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus. |
3. |
Bonnefond A et al. (2012) Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene. |
4. |
OMIM.ORG article Omim 616329 |