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xanthine dehydrogenase
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Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I
2012 |
1. lékařská fakulta
publication
Xanthine oxidase gene variants and their association with blood pressure and incident hypertension: a population study
2016 |
Lékařská fakulta v Plzni
publication
Modern diagnostic approach to hereditary xanthinuria
2015 |
1. lékařská fakulta
publication
Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)
2018 |
1. lékařská fakulta