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

Lignende værker

• 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)
• Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers
  af: Stanik, Juraj, et al.
  Udgivet: (2007)
• Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes
  af: de Wet, Heidi, et al.
  Udgivet: (2007)
• Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes
  af: Bowman, Pamela, et al.
  Udgivet: (2021)
• Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K(ATP) Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes
  af: Männikkö, Roope, et al.
  Udgivet: (2011)