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Glucokinase mutations, insulin secretion, and diabetes mellitus.Academic Article Why?
Bell, GraemePerson Why?
Insulin gene mutations as a cause of permanent neonatal diabetes.Academic Article Why?
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.Academic Article Why?
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.Academic Article Why?
In celebration of a century with insulin - Update of insulin gene mutations in diabetes.Academic Article Why?
Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.Academic Article Why?
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.Academic Article Why?
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.Academic Article Why?
Successful transition from insulin to sulfonylurea therapy in a patient with monogenic neonatal diabetes owing to a KCNJ11 F333L [corrected] mutation.Academic Article Why?
Greeley, Siri Atma W.Person Why?
Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family.Academic Article Why?
Use of in vitro DNA amplification to screen family members for an insulin gene mutation.Academic Article Why?
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.Academic Article Why?
Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family.Academic Article Why?
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