Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency

Ítems similars

• GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency
  per: De Franco, Elisa, et al.
  Publicat: (2013)
• Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus
  per: Sansbury, Francis H, et al.
  Publicat: (2015)
• Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus
  per: Sansbury, Francis H, et al.
  Publicat: (2015)
• A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency
  per: Nicolino, Marc, et al.
  Publicat: (2010)
• 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
  per: Patch, A.M., et al.
  Publicat: (2007)