Imbalanced substrate specificity of mutant β-galactosidase in patients with Morquio B disease

Author:

Okumiya Toshika,Sakuraba Hitoshi,Kase Ryoichi,Sugiura Tetsuro

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference28 articles.

1. β-Galactosidase deficiency (β-galactosidosis): GM1-gangliosidosis and Morquio B disease;Suzuki,2001

2. Galactosialidosis;d’Azzo,2001

3. Molecular defect in combined β-galactosidase and neuraminidase deficiency in man;d’Azzo;Proc. Natl. Acad. Sci. USA,1982

4. Cloning, sequencing, and expression of cDNA for human β-galactosidase;Oshima;Biochem. Biophys. Res. Commun.,1988

5. β-Galactosidase-deficient human fibroblasts: uptake and processing of the exogenous precursor enzyme expressed by stable transformant COS-1 cells;Oshima;Hum. Genet.,1990

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