Oculocutaneous albinism type 3

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

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Topic mentions per year

2001-2013
01220012013

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