Article
The clinical spectrum of albinism in humans.
Molecular medicine today - 1 Aug 1996
Oetting W S, Brilliant M H, King R A
Abstract excerpt
Oculocutaneous albinism is characterized by a congenital reduction or absence of melanin pigment in the skin, hair and eyes. The reduction in the hair and skin results in a change in color but no change in the development or function of these tissues, while the absence of melanin pigment in the e...
Topics
- Albinism, Oculocutaneous
- Animals
- Carrier Proteins
- Chromosome Mapping
- Genetic Linkage
- Humans
- Melanins
- Membrane Proteins
- Membrane Transport Proteins
- Monophenol Monooxygenase
- Mutation
- X Chromosome
