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1 eutic strategy for the clinical treatment of cystinuria.
2 est that 4F2-lc6 is a new candidate gene for cystinuria.
3 ove the diagnosis and clinical management of cystinuria.
4 fective in vivo in a knockout mouse model of cystinuria.
5 ding/trafficking defects that lead to type I cystinuria.
6 ughput, cost-effective diagnostic method for cystinuria, and for point-of-care clinical monitoring.
7 formation in the Slc3a1(-/-) mouse model of cystinuria by increasing the solubility of urinary cysti
9 hree conditions (albinism, alkaptonuria, and cystinuria) have been identified, but the mutations resp
16 acid transporter that is associated with the cystinuria-related type II membrane glycoprotein, rBAT (
17 studies of patients suffering from hypotonia-cystinuria syndrome (HCS) have revealed a deletion of a
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