AAV-Mediated Gene Delivery in Adult GM1-Gangliosidosis Mice Corrects Lysosomal Storage in CNS and Improves Survival

BACKGROUND: GM1-gangliosidosis is a glycosphingolipid (GSL) lysosomal storage disease caused by a genetic deficiency of acid β-galactosidase (βgal), which results in the accumulation of GM1-ganglioside and its asialo-form (GA1) primarily in the CNS. Age of onset ranges from infancy to adulthood, and...

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Detalles Bibliográficos
Autores principales: Baek, Rena C., Broekman, Marike L. D., Leroy, Stanley G., Tierney, Laryssa A., Sandberg, Michael A., d'Azzo, Alessandra, Seyfried, Thomas N., Sena-Esteves, Miguel
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956705/
https://www.ncbi.nlm.nih.gov/pubmed/20976108
http://dx.doi.org/10.1371/journal.pone.0013468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956705/
https://www.ncbi.nlm.nih.gov/pubmed/20976108
http://dx.doi.org/10.1371/journal.pone.0013468

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