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Zou AP, Nithipatikom K, Li PL, et al
The clinically normal heterozygous carriers for this disease have about half of the normal glutathione synthetase activity, as predicted, but have normal clinical phenotypes, cellular glutathione levels, and 5-oxoproline excretion (53)
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BJU Int 2000;85(1):8794
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These TPK1 mRNAs encode a total of six different protein isoforms
