A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis

Am J Med Genet A. 2010 Oct;152A(10):2664-5. doi: 10.1002/ajmg.a.33648.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child
  • Fatty Acid Transport Proteins / genetics*
  • Humans
  • Hyperkeratosis, Epidermolytic / genetics*
  • Infant, Newborn
  • Infant, Premature
  • Male
  • Mutation*
  • Mutation, Missense
  • Remission, Spontaneous

Substances

  • Fatty Acid Transport Proteins
  • SLC27A4 protein, human