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xanthine oxidase deficiency
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Curated Studies
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OMIM - Xanthinuria
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Literature
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A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.
A case of hereditary xanthinuria type 1 accompanied by bilateral renal calculi.
Identification of a xanthinuria type I case with mutations of xanthine dehydrogenase in an Afghan ch…
Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecul…
Xanthinuria type I with a novel mutation of xanthine dehydrogenase.
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A Natural History Study of Molybdenum Cofactor and Isolated Sulfite Oxidase Deficiencies
Study of ORGN001 (Formerly ALXN1101) in Neonates, Infants and Children With Molybdenum Cofactor Defi…
RP-3500 and Olaparib in DNA Damage Repair Pathway Deficient Relapsed/Refractory Chronic Lymphocytic …
Study of Vitamin D and Uric Acid Lowering on Kidney and Blood Vessel Function
Phase 1 Single Dose Study of ALXN1101 in Healthy Volunteers
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