Oculocutaneous albinism type 3
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Note Oculocutaneous Albinism (OCA) is a group of congenital developmental disorder characterized by complete or partial loss of… (More)
- Cell Biochemistry and Biophysics
Oculocutaneous albinism (OCA) is a genetic disease characterized by the reduction or deficiency of melanin in eyes, skin, and… (More)
To use a systems genetics approach to construct and analyze co-expression networks that are causally linked to mutations… (More)
- Pigment cell research
Tyrosinase-related protein 1 (Tyrp1) is a melanocyte-specific gene product involved in eumelanin synthesis. Mutations in the… (More)