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Cell 185 , 24522468e16 (2022)

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Introduction Wilsons disease (WD) is a genetic disorder inherited in an autosomal recessive manner, resulting from mutations in the ATP7B gene located on chromosome 13 (13q14.3)

Vitamin B 2 (riboflavin) is derived from two flavoprotein coenzymes: flavin adenine mononucleotide and flavin adenine dinucleotide, which are important rate-limiting factors in cellular enzymatic processes [20]