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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
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doi: 10.1016/0031-9422(89)80182-7 152 Soares PereiraT.KlyngerA.LobatoS.KeanD.TanY.CostaD.et al
It stimulates fat breakdown and inhibits the formation of new ones
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