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Similarly, O 2 radicals attack FeS centres in enzymes, making them inactive forever

Abstract Combined methylmalonic acidemia and homocystinuria, cblC type, is an inborn error of intracellular cobalamin metabolism with a wide spectrum of clinical manifestations that is stated to be the most common inherited disorder of cobalamin metabolism

An overview comparing two widely studied research peptides, focusing on molecular design, research methodologies, and analytical differences