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1 Introduction Hepatolenticular degeneration, also known as Wilsons disease (WD), is an autosomal recessive inheritance disorder of copper metabolism with a global prevalence of about 1/100,0003/100,000 ( via biliary tract and intestinal tract ( via bile is reduced, resulting in the deposition of copper ions in the liver

In addition, FeMn-DA/NC exhibits maximum strength at approximately 4.8 1 , indicating a MnN structure

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It demonstrated that the lipolytic activity of GH localizes to the C-terminal part and that a synthetic fragment can reproduce this activity without the other GH effects