Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660)

Clin Genet. 2007 Feb;71(2):183-6. doi: 10.1111/j.1399-0004.2007.00740.x.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Amino Acid Sequence
  • Base Sequence
  • DNA / genetics
  • Female
  • Humans
  • Lamin Type A / chemistry
  • Lamin Type A / genetics*
  • Lipodystrophy, Familial Partial / classification
  • Lipodystrophy, Familial Partial / genetics*
  • Male
  • Middle Aged
  • Mutation, Missense*
  • Phenotype

Substances

  • LMNA protein, human
  • Lamin Type A
  • DNA