Five novel mutations in tyrosinase gene of Japanese and Indian patients with oculocutaneous albinism type I (OCA1)

J Invest Dermatol. 2005 Aug;125(2):397-8. doi: 10.1111/j.0022-202X.2005.23815.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Albinism, Oculocutaneous / genetics*
  • Child, Preschool
  • Fatal Outcome
  • Female
  • Humans
  • India
  • Infant
  • Japan
  • Male
  • Monophenol Monooxygenase / genetics*
  • Point Mutation*

Substances

  • Monophenol Monooxygenase