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Finally, our findings are based on a manufacturing approach that depletes leukapheresis products of CD14+ monocytes and CD25+ Tregs, followed by positive selection of CD62L + T cells, and should not be generalized to other manufacturing approaches without further experimental support

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Similar content being viewed by others Introduction Fabry disease is a rare X-linked inherited disorder that causes defects in the glycosphingolipid metabolic pathway that result from the deficient or absent activity of the lysosomal enzyme -galactosidase A (-Gal A) 1

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