Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

J Dermatol Sci. 2015 Apr;78(1):82-5. doi: 10.1016/j.jdermsci.2015.02.006. Epub 2015 Feb 19.
No abstract available

Keywords: Autosomal recessive congenital ichthyosis; Malaysia; Mutation analysis.

Publication types

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

MeSH terms

  • ATP-Binding Cassette Transporters / genetics*
  • Arachidonate 12-Lipoxygenase / genetics*
  • Asian People / genetics
  • DNA Mutational Analysis
  • Gene Frequency
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Humans
  • Ichthyosis, Lamellar / diagnosis
  • Ichthyosis, Lamellar / ethnology
  • Ichthyosis, Lamellar / genetics*
  • Japan / epidemiology
  • Malaysia / epidemiology
  • Mutation*
  • Phenotype
  • Risk Factors

Substances

  • ABCA12 protein, human
  • ATP-Binding Cassette Transporters
  • Genetic Markers
  • ALOX12B protein, human
  • Arachidonate 12-Lipoxygenase