Chromosomal localization of the human gl
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Christine Morris; Nora Heisterkamp; John Groffen; Julian C. Williams; Ilkka Mono
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Article
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1992
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Springer
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English
⚖ 268 KB
Glycoasparaginase cleaves the N-glycosidic linkage between asparagine and N-acetylglucosamine in the degradation of glycoproteins. In humans, a deficient activity of glycoasparaginase results in accumulation of glycoasparagines, causing the lysosomal storage disease aspartylglycosaminuria. Recombina