Mutation of Human Molybdenum Cofactor Sulfurase Gene Is Responsible for Classical Xanthinuria Type II
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference23 articles.
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2. Hereditary xanthinuria;Simmonds,1995
3. Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency;Johnson,1995
4. Two siblings with classical xanthinuria type 1: Significance of allopurinol loading test;Ichida;Intern. Med.,1998
5. Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxypurinol;Reiter;Clin. Chim. Acta,1990
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