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Supplementary Figure 3 Effect of BAY 43-9006 on eryptosis levels of nave and P

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This reduces ambiguity during internal review and improves continuity when a laboratory needs to confirm exactly which reference input was used in a given experiment or method-development series

146,147,148 Tuberous sclerosis is an autosomal dominant disorder arising from heterozygous mutations in the TSC1 and TSC2 genes that is commonly associated with deficits in long-term and working memory, intellectual disability, and ASD