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The current treatment of cystinosis uses cysteamine, which when taken up in the cell, moves to the lysosome, and forms cysteine-cysteamine mixed disulphides, that lead to the depletion of cystine since this disulphide can be effluxed out of the lysosome through a different lysosomal PQ-loop efflux pump, the PQLC2 transporter 5
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