LMNA mutations in atypical Werner's syndrome

Lancet. 2003 Nov 8;362(9395):1585; author reply 1586. doi: 10.1016/S0140-6736(03)14760-5.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Humans
  • Lamin Type B / genetics*
  • Lipodystrophy / diagnosis
  • Lipodystrophy / genetics*
  • Male
  • Mutation / genetics*
  • Werner Syndrome / diagnosis
  • Werner Syndrome / genetics*

Substances

  • Lamin Type B
  • lamin B1