Publication | Closed Access
Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease.
139
Citations
29
References
1991
Year
UrologyAutoimmune DiseaseGenetic DisorderGeneticsInherited Metabolic DiseaseMissense MutationPathologyMolecular GeneticsMedicineLysosomal Storage DiseaseHuman Aspartylglucosaminidase
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