Pages that link to "Q44613198"
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The following pages link to Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria (Q44613198):
Displaying 16 items.
- A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation (Q28483790) (← links)
- Xanthine urolithiasis (Q33243343) (← links)
- Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria (Q34609569) (← links)
- An unusual cause of pink diapers in an infant: Questions and Answers (Q36113673) (← links)
- An unusual cause of "pink diaper" in an infant: Answers. (Q36113752) (← links)
- Increasing recognition of the importance of aldehyde oxidase in drug development and discovery (Q37856257) (← links)
- Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans (Q38064334) (← links)
- Human disease locus discovery and mapping to molecular pathways through phylogenetic profiling. (Q39089127) (← links)
- Classical xanthinuria: a rare cause of pediatric urolithiasis (Q40586650) (← links)
- Xanthine oxidase gene variants and their association with blood pressure and incident hypertension: a population study (Q40589901) (← links)
- A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase (Q41956435) (← links)
- Kinetics of 6-Thioxanthine Metabolism by Allelic Variants of Xanthine Oxidase (Q42918840) (← links)
- Increased xanthine oxidase in the thalamus and putamen in depression (Q43135404) (← links)
- Xanthinuria type I: a rare cause of urolithiasis (Q79370770) (← links)
- An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt (Q89769210) (← links)
- Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient (Q94953154) (← links)