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Page 1
Characterization of a Compound Heterozygous SLC2A9 Mutation That Causes Hypouricemia.
Biomedicines. 2021 Sep 6;9(9):1172. doi: 10.3390/biomedicines9091172.
Biomedicines. 2021.
PMID: 34572357
Free PMC article.
Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
Nandlal L, Winkler CA, Bhimma R, Cho S, Nelson GW, Haripershad S, Naicker T.
Nandlal L, et al. Among authors: cho s.
Eur J Pediatr. 2022 Oct;181(10):3595-3606. doi: 10.1007/s00431-022-04581-x. Epub 2022 Aug 3.
Eur J Pediatr. 2022.
PMID: 35920919
Free PMC article.
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Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population.
Stiburkova B, Bohatá J, Pavelcová K, Tasic V, Plaseska-Karanfilska D, Cho SK, Potočnaková L, Šaligová J.
Stiburkova B, et al.
Biomedicines. 2021 Nov 3;9(11):1607. doi: 10.3390/biomedicines9111607.
Biomedicines. 2021.
PMID: 34829836
Free PMC article.
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