Sortilin mediates the lysosomal targeting of cathepsins D and H
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
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3. Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5’-diphosphate-N-acetylglucosamine: glycoprotein N-acetylglucosaminylphosphotransferase activity;Reitman;J. Clin. Invest.,1981
4. Identification of a variant of mucolipidosis III (pseudo-Hurler polydystrophy): a catalytically active N-acetylglucosaminylphosphotransferase that fails to phosphorylate lysosomal enzymes;Varki;Proc. Natl. Acad. Sci. USA,1981
5. Deficiency of UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients;Waheed;Biochem. Biophys. Res. Commun.,1982
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