A novel mutation of the FECH gene in a Chinese family with erythropoietic protoporphyria

J Dermatol Sci. 2007 Nov;48(2):145-7. doi: 10.1016/j.jdermsci.2007.07.004. Epub 2007 Aug 27.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child
  • China
  • Female
  • Ferrochelatase / genetics*
  • Humans
  • Male
  • Point Mutation
  • Protoporphyria, Erythropoietic / genetics*

Substances

  • Ferrochelatase