Two genetically different MU-NANA neuraminidases in human leucocytes
- 1 December 1983
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 117 (2), 470-478
- https://doi.org/10.1016/0006-291x(83)91224-x
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Lysosomal sialidase deficiency in sialidosis with partial β-galactosidase deficiencyBiochimica et Biophysica Acta (BBA) - General Subjects, 1983
- Purification of acid β-galactosidase and acid neuraminidase from bovine testis: Evidence for an enzyme complexBiochemical and Biophysical Research Communications, 1982
- Neuraminidase deficiency and accumulation of sialic acid in lymphocytes in adult type sialidosis with partial β‐galactosidase deficiencyAnnals of Neurology, 1982
- Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiencyBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1982
- Genetic heterogeneity in human neuraminidase deficiencyNature, 1980
- Mucolipidosis type IV: Ganglioside sialidase deficiencyBiochemical and Biophysical Research Communications, 1979
- Oligosaccharide and Ganglioside Neuraminidase Activities of Mucolipidosis I (Sialidosis) and Mucolipidosis II (I‐Cell Disease) FibroblastsEuropean Journal of Biochemistry, 1979
- Sialidase (α‐N‐acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry‐red spots and myoclonus without dementiaClinical Genetics, 1978
- Neuraminidase deficiency in the cherry red spot-myoclonus syndromeBiochemical and Biophysical Research Communications, 1977
- ANGIOKERATOMA CORPORIS DIFFUSUM AND LYSOSOMAL ENZYME DEFICIENCYThe Lancet, 1974