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Within GSTs, the GSH-conjugating site lies in a Trx-like domain (Atkinson et al., 2009)

Those who had genotyping data available between inception and December 2022 and were identified to be homozygous for the HFE C282Y mutation were included in the study

To match this call for inclusivity, trial design must also evolve, adopting adaptive and master protocols that reflect the complexity of neurodegeneration in the real world

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