Insulin Mutation Screening in 1044 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

Lignende værker

• Mutations in the ABCC8 gene encoding the SUR1 subunit of the K(ATP) channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period
  af: Patch, A.M., et al.
  Udgivet: (2007)
• Effective treatment with oral sulfonylureas in patients with diabetes due to SUR1 Mutations
  af: Rafiq, Meena, et al.
  Udgivet: (2008)
• Insulin gene mutations as a cause of permanent neonatal diabetes
  af: Støy, Julie, et al.
  Udgivet: (2007)
• Mutations in K(ATP) Channel Genes cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood
  af: Flanagan, Sarah E., et al.
  Udgivet: (2007)
• Permanent Neonatal Diabetes Caused by Dominant, Recessive, or Compound Heterozygous SUR1 Mutations with Opposite Functional Effects
  af: Ellard, Sian , et al.
  Udgivet: (2007)