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Journal Abstract Search

161 related items for PubMed ID: 8812740

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  • 8. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
    Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O.
    J Clin Invest; 1997 May 15; 99(10):2391-7. PubMed ID: 9153281
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  • 10. Molybdenum cofactor deficiency.
    Arnold GL, Greene CL, Stout JP, Goodman SI.
    J Pediatr; 1993 Oct 15; 123(4):595-8. PubMed ID: 8410516
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  • 12. Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor.
    Bonioli E, DiStefano A, Palmieri A, Bertola A, Bellini C, Caruso U, Fantasia AR, Minniti G, Dorche C.
    J Inherit Metab Dis; 1996 Oct 15; 19(5):700-1. PubMed ID: 8892030
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  • 15. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
    Ichida K, Matsumura T, Sakuma R, Hosoya T, Nishino T.
    Biochem Biophys Res Commun; 2001 Apr 20; 282(5):1194-200. PubMed ID: 11302742
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  • 19. Cell biology of molybdenum.
    Mendel RR.
    Biofactors; 2009 Apr 20; 35(5):429-34. PubMed ID: 19623604
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