Associated Papers
Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects.
Zhou Z et al.
Molecular Genetics & Genomic Medicine, 2019
31131560 (PubMed )
Supplement: MGG3-7-e00722-s002.xlsx › sheet_2
Vanishing urate, acute kidney injury episodes and a homozygous SLC2A9 mutation.
Androvitsanea A et al.
International Urology and Nephrology, 2015
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