Further reading on the different MODY subtypes

• Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation, Diabetic Medicine, Murphy R et al 2008. _{Note that you may need to pay for this article, unless you are accessing this from an institution which may have licensing arrangements put in place.}

• HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum, Nat Rev Nephrol, Clissold RL et al 2015

• Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation, Diabetes Care, Chakera AJ et al 2015

• Genetic cause of hyperglycaemia and response to treatment in diabetes, The Lancet, Pearson ER et al 2003

To find out more about the risk of cardiovascular mortality in patients with HNF1A MODY, please see:

• Increased all-cause and cardiovascular mortality in monogenic diabetes as a result of mutations in the HNF1A gene, Steele et al Diabet Med 2010 _{Note that you may need to pay for this article, unless you are accessing this from an institution which may have licensing arrangements put in place.}