Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family

Diabet Med. 2001 Apr;18(4):334-6. doi: 10.1046/j.1464-5491.2001.00429-2.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • DNA, Mitochondrial / genetics*
  • Deafness / genetics*
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetes Mellitus, Type 2 / genetics*
  • Female
  • Genomic Imprinting
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Pedigree
  • Point Mutation*

Substances

  • DNA, Mitochondrial