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Whole-animal senescent cytotoxic T cell removal using antibodies linked to magnetic nanoparticles
Liberty Hosfeld, Kathryn P
SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) (1517), an autosomal recessive disorder characterized by skeletal myopathy, progressive cardiomyopathy, hypoglycemia, and hyperammonemia
