Coincidence of a Novel KCNJ11 Missense Variant R365H With a Paternally Inherited 6q24 Duplication in a Patient With Transient Neonatal Diabetes

Gelijkaardige items

• Prevalence of Permanent Neonatal Diabetes in Slovakia and Successful Replacement of Insulin with Sulfonylurea Therapy in KCNJ11 and ABCC8 Mutation Carriers
  door: Stanik, Juraj, et al.
  Gepubliceerd in: (2007)
• Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk
  door: Vedovato, Natascia, et al.
  Gepubliceerd in: (2016)
• Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes
  door: Babiker, Tarig, et al.
  Gepubliceerd in: (2016)
• Origin of de Novo KCNJ11 Mutations and Risk of Neonatal Diabetes for Subsequent Siblings
  door: Edghill, Emma L., et al.
  Gepubliceerd in: (2007)
• Retraction for Ma et al., Glucose regulates the effects of leptin on hypothalamic POMC neurons
  door: Ashcroft, Frances M., et al.
  Gepubliceerd in: (2009)