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Article

Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical type I xanthinuria

24 Apr 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11379872
DOI: 10.1007/s004390100477

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Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical type I xanthinuriaPMID 11379872Read ↗

Xanthinuria type I with a novel mutation of xanthine dehydrogenase.Semantic proximity Read ↗

Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.Semantic proximity Read ↗

Molecular Cloning and Characterization of the Human Xanthine Dehydrogenase Gene (XDH)Semantic proximity Read ↗

Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I.Semantic proximity Read ↗

A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.Semantic proximity Read ↗

Association of Mutations Identified in Xanthinuria with the Function and Inhibition Mechanism of Xanthine OxidoreductaseSemantic proximity Read ↗

Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase): Structural analysis of the protein and chromosomal location of the geneSemantic proximity Read ↗

[Classical xanthinuria (type I and II)].Semantic proximity Read ↗

Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient.Semantic proximity Read ↗

XDH gene mutation is the underlying cause of classical xanthinuria: a second report.Semantic proximity Read ↗

[Analysis of a family with hypouricemia due to type Ⅰ xanthinuria].Semantic proximity Read ↗

Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.Semantic proximity Read ↗

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