Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I

Congenital deficiency of the lysosomal sialidase neuraminidase 1 (NEU1) causes the lysosomal storage disease, sialidosis, characterized by impaired processing/degradation of sialo-glycoproteins and sialo-oligosaccharides, and accumulation of sialylated metabolites in tissues and body fluids. Sialido...

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Detalles Bibliográficos
Autores principales: Mosca, Rosario, van de Vlekkert, Diantha, Campos, Yvan, Fremuth, Leigh E., Cadaoas, Jaclyn, Koppaka, Vish, Kakkis, Emil, Tifft, Cynthia, Toro, Camilo, Allievi, Simona, Gellera, Cinzia, Canafoglia, Laura, Visser, Gepke, Annunziata, Ida, d’Azzo, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141319/
https://www.ncbi.nlm.nih.gov/pubmed/32143456
http://dx.doi.org/10.3390/jcm9030695

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141319/
https://www.ncbi.nlm.nih.gov/pubmed/32143456
http://dx.doi.org/10.3390/jcm9030695

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