Article
Generation of a novel <i>Slc7a9</i> <sup>G105R</sup> mutant mouse identifies new biomarkers for cystinuria
2026-02-12
Abstract excerpt
Cystinuria is a rare inherited disease characterized by increased urinary cystine levels resulting in the formation of cystine stones in the urinary tract. Mutations in the genes encoding the cystine transporter complex, SLC3A1 and SLC7A9, are the primary drivers of the disease. Current mouse models used to study cystinuria rely on gene deficiency or spontaneous mutations in mice that do not accurately reflect t...
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Identifiers and source
- Literature Corpus work
- 68f42043-35ea-526c-8139-0204cab8619c
- DOI
- 10.64898/2026.02.10.705194