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Question

Albinism is due to hereditary deficiency of enzyme

A
Amylase
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B
Carbonic anhydrase
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C
Acetyl choline esterase
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D
Tyrosinase
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Solution

The correct option is D Tyrosinase
Tyrosinase is a copper-containing enzyme present in plant and animal tissues that catalyzes the production of melanin and other pigments from tyrosine by oxidation, as in the blackening of a peeled or sliced potato exposed to air. It is found inside melanosomes which are synthesized in the skin melanocytes. In humans, the tyrosinase enzyme is encoded by the TYR gene. A mutation in the tyrosinase gene resulting in impaired tyrosinase production leads to type I oculocutaneous albinism, a hereditary disorder.

So, the correct answer is 'Tyrosinase'.

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