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A growing number of publications has well documented that ROS also play a central role in various non-apoptotic forms of regulated cell death, including lysosomal cell death [84], pyroptosis [85], netotic cell death [86], necroptosis [87], parthanatos [88], ferroptosis [89], autophagic cell death [90], and oxeiptosis [91]

Additional investigations include brain magnetic resonance imaging, and the identification of ATP7B mutations [17] based on which the prevalence rate of WD is now estimated to be 1 in 7,026 people compared to 1 in 35,000-45,000 people before the advent of this molecular investigation [18]

Which strengths are available