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f’xi pazjenti, glycosaminoglycan jakkumula wkoll fil-moħħ.
in some patients glycosaminoglycan accumulates also in the brain.
Last Update: 2017-04-26
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individwi li se jieħdu sehem fil- programm se jkollhom il- glycosaminoglycan
subjects enrolled in the program will have urinary glycosaminoglycan and samples for igg antibodies routinely collected as specified in the schedule of activities.
Last Update: 2011-10-23
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glycosaminoglycan li hu responsabbli ghall- interazzjoni ma 'l eparina u sustanzi relatati, li
the second is a glycosaminoglycan binding domain responsible for the interaction with heparin and related substances, which accelerates the inhibition of thrombin.
Last Update: 2011-10-23
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mps vi hija marda eteroġena li tidher f’diversi sistemi tal-ġisem, ikkaratterizzata minn defiċjenza ta’ n- acetylgalactoasamine 4-sulfatase, hydrolase liżosomali li tikkatalizza l-idroliżi tal-porzjon ta’ sulfate ta’ glycosaminoglycan, dermatan sulfate.
mps vi is a heterogeneous and multisystemic disorder characterized by the deficiency of n-acetylgalactoasamine 4-sulfatase, a lysosomal hydrolase which catalyses the hydrolysis of sulfate moiety of the glycosaminoglycan, dermatan sulfate.
Last Update: 2017-04-26
Usage Frequency: 3
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