Cell-Mediated Immunity to NAGLU Transgene Following Intracerebral Gene Therapy in Children With Mucopolysaccharidosis Type IIIB Syndrome

Mucopolysaccharidosis type IIIB syndrome (Sanfilippo disease) is a rare autosomic recessif disorder caused by mutations in the α-N-acetylglucosaminidase (NAGLU) gene coding for a lysosomal enzyme, leading to neurodegeneration and progressive deterioration of cognitive abilities in affected children....

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Detalles Bibliográficos
Autores principales: Gougeon, Marie-Lise, Poirier-Beaudouin, Béatrice, Ausseil, Jérome, Zérah, Michel, Artaud, Cécile, Heard, Jean-Michel, Deiva, Kumaran, Tardieu, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141743/
https://www.ncbi.nlm.nih.gov/pubmed/34040605
http://dx.doi.org/10.3389/fimmu.2021.655478

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141743/
https://www.ncbi.nlm.nih.gov/pubmed/34040605
http://dx.doi.org/10.3389/fimmu.2021.655478

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