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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

Semantic Scholar uses AI to extract papers important to this topic.
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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