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References Calef Snchez-Trasvia, Coronel-Meneses D, Aleyda Margarita Escobar-Fernndez, Mayolo-Deloisa K
In the absence of rigorous pharmacokinetic studies, protocol-design guidance relies on effect-equivalence: what oral dose produces equivalent endpoint outcomes to a parenteral reference dose
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OMIM #250940), decreased function of the reactivating enzyme methionine synthase reductase (cblE
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