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Obstructive sleep apnea and comorbidities: a dangerous liaison

PD and DLB are the most studied diseases of -syn at present [28, 29]

During the pathogenesis of OA, JUN directly binds to the promoter of NCOA4 and initializes its transcription, increasing ferritinophagy degradation, leading to ferroptosis and extracellular matrix degradation in chondrocytes