A comparative study of the accumulated sialic acid-containing oligosaccharides from cultured human galactosialidosis and sialidosis fibroblasts

Author:

Van Pelt Johannes,Kamerling Johannis P.,Vliegenthart Johannes F.G.,Hoogeveen AndréT.,Galjaard Hans

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference26 articles.

1. Sialidosis: a review of human neuraminidase deficiency;Lowden;Am J Hum Genet,1979

2. Macular cherry red spots and myoclonus with dementia: coexistent neuraminidase and β-galactosidase deficiencies;Wenger;Biochem Biophys Res Commun,1978

3. Correction of combined β-galactosidase/ neuraminidase deficiency in human fibroblasts;Hoogeveen;Biochem Biophys Res Commun,1981

4. Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiency;Van Diggelen;Biochim Biophys Acta,1982

5. Molecular defect in combined β-galactosidase and neuraminidase deficiency in man;D'Azzo,1982

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