Hutchinson-Gilford progeria syndrome: report of 2 cases and a novel LMNA mutation of HGPS in China

J Am Acad Dermatol. 2013 Oct;69(4):e175-6. doi: 10.1016/j.jaad.2011.07.002.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Biopsy, Needle
  • China
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Immunohistochemistry
  • Infant
  • Lamin Type A / genetics*
  • Progeria / genetics*
  • Progeria / pathology*
  • Rare Diseases

Substances

  • LMNA protein, human
  • Lamin Type A