Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
MODY13 is an autosomal dominant early-onset type 2 diabetes caused by mutations of the KCNJ11 gene.
| 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. 
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| 2. |
Prudente S et al. (2015) Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.
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| 3. |
Bonnefond A et al. (2012) Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.
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| 4. |
OMIM.ORG article Omim 616329
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