Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblings.

Samankaltaisia teoksia

• Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.
  Tekijä: Flanagan, SE, et al.
  Julkaistu: (2006)
• KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.
  Tekijä: Gloyn, A, et al.
  Julkaistu: (2006)
• Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel.
  Tekijä: Gloyn, A, et al.
  Julkaistu: (2004)
• Neonatal diabetes caused by homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensititvity markedly affect diabetes risk
  Tekijä: Vedovato, N, et al.
  Julkaistu: (2016)
• KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.
  Tekijä: Massa, O, et al.
  Julkaistu: (2005)