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Nearly half of the people with RLS also have a family member with the condition

Research indicates that CTNNB1 gene mutations are present in about 20%-40% of HCC cases, and this mutation occurs more frequently in HCC cases related to Hepatitis C virus (HCV) infection than in HCC cases related to Hepatitis B virus (HBV) infection (65, 66)

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Additionally, we reviewed relevant research on the modulation of ferroptosis signaling pathways as a potential approach for developing antidepressant interventions

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