Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene

Diabetologia. 2004 Apr;47(4):753-6. doi: 10.1007/s00125-004-1360-4.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Female
  • Heterozygote
  • Humans
  • Lamin Type A
  • Lamins / genetics*
  • Lipodystrophy / complications*
  • Lipodystrophy / genetics*
  • Lipodystrophy / pathology
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Mutation / physiology*

Substances

  • LMNA protein, human
  • Lamin Type A
  • Lamins