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</html><description>A plasma copper protein that functions as an enzyme and results in the formation of hallucination producing products from natural amines ceruplasmin.A copper-containing globulin in blood plasma with a molecular weight of 150,000 and eight copper atoms. It catalyzes the oxidation of amines, phenols, and ascorbic acid. It is reduced in amount in Wilson&#x2019;s disease (hepatolenticular disease).A protein with which most of the blood&#x2019;s copper is combined. Elevated levels may occur in liver disease, leukemia, and heart attack; decreased levels occur in other forms of liver disease and in nutritional deficiencies.A copper-containing protein present in blood plasma. Congenital deficiency of ceruloplasmin leads to abnormalities of the brain and liver.A blue glycoprotein to which most of the copper in the blood is attached. It is decreased in Wilson&#x2019;s disease.There exists a protein traversing through the bloodstream that binds itself to copper and facilitates its transportation.</description></oembed>
