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Positive Exposure Ambassadors’ Real Life Stories is a ground-breaking educational tool invites students to learn about their peers living with genetic, physical and behavioral differences through an image gallery and safe online blog.

DHICA oxidase is a catalytic step downstream from tyrosinase in the biosynthesis of melanin from tyrosine.

The function of Oculocutaneous albinism type 7 results from mutations in an unknown gene, which maps to band 10q22.2-3 and is inherited as an autosomal recessive trait.

The proteins/gene products (and respective gene) affected in each form of oculocutaneous albinism are as follows Oculocutaneous albinism type 1 results from mutations in the tyrosinase gene, which maps to band 11q14-3 and is inherited as an autosomal recessive trait.

The tyrosinase gene encodes an enzyme that initiates the synthesis of melanin using the substrate tyrosine.

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Whether you chose albinism as a topic, or whether it was assigned to you, our goal is to provide accurate information about this rare genetic condition.

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