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Description
Most of these trials have focused on intravenous administration of the supplement
17.9%) and pregestational diabetes (8.7% vs
2-Hydroxyglutarate produced by neomorphic IDH mutations suppresses homologous recombination and induces PARP inhibitor sensitivity
Clinical studies have validated safety and efficacy with minimal adverse effects when using advanced transdermal delivery systems
10.1007/s00253-015-6561-x Appl
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