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ARID1A is a member of the SWI/SNF family, and the inhibition of GLS1 by SWI/SNF is weakened in OCCC with ARID1A mutation, which promotes Gln utilization and metabolism IN tumor cells

Figure 6 Figure 7 8 Epilepsy characteristics caused by different mitochondrial complex dysfunctions The classification of mitochondrial diseases is based on several factors, including the affected tissues and organs, the dysfunction of respiratory chain enzyme complexes, and the types of gene mutations involved