Systemic and neurologic abnormalities distinguish the lysosomal disorders sialidosis and galactosialidosis in mice
Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis
Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex
Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement
Long-term follow-up of metachronous marrow-kidney transplantation in severe type II sialidosis: what does success mean?
Cloning of the cDNA and Gene Encoding Mouse Lysosomal Sialidase and Correction of Sialidase Deficiency in Human Sialidosis and Mouse SM/J Fibroblasts
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another name for mucolipidosis I.
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