Skip to search formSkip to main contentSkip to account menu

Oculocutaneous albinism type 3

Known as: Albinism 3, Albinism, oculocutaneous, type 3 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Note Oculocutaneous Albinism (OCA) is a group of congenital developmental disorder characterized by complete or partial loss of… 
2011
2011
Oculocutaneous albinism (OCA) is a genetic disease characterized by the reduction or deficiency of melanin in eyes, skin, and… 
2011
2011
Purpose To use a systems genetics approach to construct and analyze co-expression networks that are causally linked to mutations… 
Review
2001
Review
2001
Tyrosinase-related protein 1 (Tyrp1) is a melanocyte-specific gene product involved in eumelanin synthesis. Mutations in the…