Mutations in IAPP and NEUROG3 genes are not a common cause of permanent neonatal/infancy/childhood-onset diabetes

Diabet Med. 2009 Jun;26(6):660-1. doi: 10.1111/j.1464-5491.2009.02726.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amyloid / genetics*
  • Autoantibodies
  • Basic Helix-Loop-Helix Transcription Factors
  • Child
  • Child, Preschool
  • Diabetes Mellitus, Type 1 / genetics*
  • Humans
  • Immunologic Factors
  • Infant
  • Infant, Newborn
  • Islet Amyloid Polypeptide
  • Mutation / genetics*
  • Nerve Tissue Proteins

Substances

  • Amyloid
  • Autoantibodies
  • Basic Helix-Loop-Helix Transcription Factors
  • Immunologic Factors
  • Islet Amyloid Polypeptide
  • NEUROG3 protein, human
  • Nerve Tissue Proteins