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[Two mutated amino acid transporter genes, however, have been recently identified as responsible for cystinuria.Mutations in the SLC3A1 gene. encoding for the heavy subunit of the transporter protein rBAT, were associated with type I cystinuria, whereas type II and III cystinuria were associated with mutations in the SLC7A9 gene, encoding for a light subunit of rBAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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