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- W2601187782 abstract "Cystinuria is a rare genetic disorder caused by mutations in the genes that encode the two subunits of amino acid transport, resulting in failure of absorption of filtered dibasic amino acids including cystine in the proximal tubules" @default.
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- W2601187782 date "2016-11-01" @default.
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- W2601187782 title "The challenges of cystinuria in the twenty-first century - a mini review" @default.
- W2601187782 doi "https://doi.org/10.29245/2572-9411/2016/3.1047" @default.
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