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Modern diagnostic approach to hereditary xanthinuria.
Urolithiasis. 2015 Feb;43(1):61-7. doi: 10.1007/s00240-014-0734-4. Epub 2014 Nov 6.
Urolithiasis. 2015.
PMID: 25370766
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
Mancikova A, Krylov V, Hurba O, Sebesta I, Nakamura M, Ichida K, Stiburkova B.
Mancikova A, et al. Among authors: hurba o.
Clin Exp Nephrol. 2016 Aug;20(4):578-584. doi: 10.1007/s10157-015-1186-z. Epub 2015 Oct 24.
Clin Exp Nephrol. 2016.
PMID: 26500098
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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.
Hurba O, Mancikova A, Krylov V, Pavlikova M, Pavelka K, Stibůrková B.
Hurba O, et al.
PLoS One. 2014 Sep 30;9(9):e107902. doi: 10.1371/journal.pone.0107902. eCollection 2014.
PLoS One. 2014.
PMID: 25268603
Free PMC article.
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