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Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
Makris et al., 2013), however, cellular and molecular mechanisms underlying intracellular copper transportation in chondrocytes are not yet clearly understood
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In particular, USP22 raised GSH content and reduced the occurrence of ferroptosis in cardiomyocytes by activating the Sirt1-p53/SLC7A11 axis [252]
Our guide on how long GLP-1 fatigue lasts walks through the typical timeline
