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aspartylglycosaminuria
(phenotype)
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AGA
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Peptidase T2, asparaginase 2
MODULE_211
Threonine proteases
Nucleophile aminohydrolases, N-terminal
ROZANOV_MMP14_TARGETS_DN
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Mouse Phenotypes - Autosomal recessive hereditary disorder
OMIM - Congenital disorder
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Most Relevant Literature
A new horizon in the phosphorylated sites of AGA: the structural impact of C163S mutation in asparty…
Pre-clinical Gene Therapy with AAV9/AGA in Aspartylglucosaminuria Mice Provides Evidence for Clinica…
Aspartylglucosaminuria: Clinical Presentation and Potential Therapies.
Analysis of genetic variant in a child with Aspartylglucosaminuria].
Aspartylglycosaminuria: a review.
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There were no clinical trials for aspartylglycosaminuria
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