MOCOS protein, human

Known as: HMCS protein, human, human molybdenum cofactor sulfurase, molybdenum cofactor sulfurase, human 
 
National Institutes of Health

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2007
2007
Classical xanthinuria type II is an autosomal recessive disorder characterized by deficiency of xanthine dehydrogenase and… (More)
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2001
2001
Drosophila ma-l gene was suggested to encode an enzyme for sulfuration of the desulfo molybdenum cofactor for xanthine… (More)
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