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The teams findings illuminate how mutations in SLC33A1 disrupt this glutathione transport pathway, offering a molecular explanation for neurodevelopmental disorders such as Huppke-Brindle Syndrome, characterized by severe intellectual disability and progressive neurodegeneration
doi: 97
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The Thioredoxin system is one of the main redox buffer systems in the body, which plays a key role in the transduction of redox signals (Shchedrina et al., 2010)
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