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Occurrence in Brain Lysosomes of a Sialidase Active on Ganglioside

✍ Scribed by Amelia Fiorilli; Bruno Venerando; Carola Siniscalco; Eugenio Monti; Roberto Bresciani; Luigi Caimi; Augusto Preti; Guido Tettamanti

Book ID
111175428
Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
938 KB
Volume
53
Category
Article
ISSN
0022-3042

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## Communicated by Georgia Chenevix-Trench Sialidosis is an autosomal recessive disease resulting from a deficiency of lysosomal sialidase. Type II sialidosis is a rare disease characterized clinically by hydrops fetalis, hepatosplenomegaly, and severe psychomotor retardation. Genomic DNA from fou