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Oculocutaneous albinism type 3

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

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Broader (1)

Albinism, Oculocutaneous

Papers overview

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2013
2013
Atlas of Genetics and Cytogenetics in Oncology and Haematology Oculocutaneous Albinism
Note Oculocutaneous Albinism (OCA) is a group of congenital developmental disorder characterized by complete or partial loss of… Expand
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2011
2011
Oculocutaneous Albinism Type 3 (OCA3): Analysis of Two Novel Mutations in TYRP1 Gene in Two Chinese Patients
Oculocutaneous albinism (OCA) is a genetic disease characterized by the reduction or deficiency of melanin in eyes, skin, and… Expand
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2011
2011
Complex interactions of Tyrp1 in the eye
PURPOSE To use a systems genetics approach to construct and analyze co-expression networks that are causally linked to mutations… Expand
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Review
2001
Review
2001
Tyrp1 and oculocutaneous albinism type 3.
Tyrosinase-related protein 1 (Tyrp1) is a melanocyte-specific gene product involved in eumelanin synthesis. Mutations in the… Expand
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