Molecular basis of Kir6.2 mutations causing neonatal diabetes and neonatal diabetes with neurological features

Antzeko izenburuak

• Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
  nork: Proks, P, et al.
  Argitaratua: (2004)
• Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms.
  nork: Männikkö, R, et al.
  Argitaratua: (2010)
• Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes.
  nork: Girard, C, et al.
  Argitaratua: (2006)
• Permanent neonatal diabetes caused by an in-frame deletion in the N-terminus of Kir6.2
  nork: Craig, T, et al.
  Argitaratua: (2008)
• Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions.
  nork: Tammaro, P, et al.
  Argitaratua: (2005)