Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
MODY10 is an autosomal dominant early-onset type 2 diabetes caused by mutations of the proinsulin gene (INS).
| 1. |
Edghill EL et al. (2008) Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. 
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| 2. |
Molven A et al. (2008) Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
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| 3. |
OMIM.ORG article Omim 613370
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