Human α-fucosidase
Author:
Publisher
Elsevier BV
Reference13 articles.
1. A NEW MUCOPOLYSACCHARIDE LIPIDSTORAGE DISEASE?
2. Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolism
3. Electrophoretic forms of human liver α-l-fucosidase and their relationship to fucosidosis (mucopolysaccharidosis F)
4. Isozymes of human α-l-fucosidase detectable by starch gel electrophoresis
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1. Intrafamilial variability in fucosidosis;Clinical Genetics;2008-06-28
2. Glycolipid and Glycoprotein Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
3. Low fibroblast fucosidase activity: false-positive diagnosis of fucosidosis in a patient with pseudohypoparathyroidism;Journal of Inherited Metabolic Disease;1987-06
4. α-L-fucosidase in the reproductive organs and seminal plasma of the bull;Biochimica et Biophysica Acta (BBA) - General Subjects;1986-01-15
5. Isoelectric forms of α-l-fucosidase in mouse teratocarcinoma-derived cell lines;Developmental Biology;1985-10
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