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Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
- Published in:
- Clinical & Experimental Nephrology, 2016, v. 20, n. 4, p. 578, doi. 10.1007/s10157-015-1186-z
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- Article
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 Gout.
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- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107902
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- Article
Modern diagnostic approach to hereditary xanthinuria.
- Published in:
- Urolithiasis, 2015, v. 43, n. 1, p. 61, doi. 10.1007/s00240-014-0734-4
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- Article