Publications
- Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 22016 | Faculty of Science, First Faculty of Medicine
- Modern diagnostic approach to hereditary xanthinuria2015 | First Faculty of Medicine
- Complex Analysis of Urate Transporters SLC2A9, SLC22A12 and Functional Characterization of Non-Synonymous Allelic Variants of GLUT9 in the Czech Population: No Evidence of Effect on Hyperuricemia and Gout2014 | Faculty of Science, First Faculty of Medicine
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