Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

Ítems similars

• Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features
  per: Proks, P, et al.
  Publicat: (2005)
• Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
  per: Proks, P, et al.
  Publicat: (2004)
• Permanent neonatal diabetes caused by an in-frame deletion in the N-terminus of Kir6.2
  per: Craig, T, et al.
  Publicat: (2008)
• Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.
  per: Gloyn, A, et al.
  Publicat: (2004)
• Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.
  per: Sagen, J, et al.
  Publicat: (2004)