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Results 1 - 4 of 4 for Cofactor
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  1. Molybdenum cofactor deficiency 
    Molybdenum cofactor deficiency is a rare condition characterized by brain dysfunction (encephalopathy) that worsens over time. Babies with this condition appear ...
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency - Genetics
  2. Methylmalonic acidemia with homocystinuria 
    ... acids, lipids, and cholesterol. AdoCbl is called a cofactor because it helps the enzyme carry out its function. MeCbl is also a cofactor, but for another enzyme that converts homocysteine to ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  3. Hereditary xanthinuria 
    ... provides instructions for making an enzyme called molybdenum cofactor sulfurase. This enzyme is necessary for the normal ... Hosoya T, Nishino T. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type ...
    https://medlineplus.gov/genetics/condition/hereditary-xanthinuria - Genetics
  4. Isolated sulfite oxidase deficiency 
    ... Sadek AA, Gleeson JG, Abdel Hamid MS. Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular ...
    https://medlineplus.gov/.../isolated-sulfite-oxidase-deficiency - Genetics