Human iPSC-based neurodevelopmental models of globoid cell leukodystrophy uncover patient- and cell type-specific disease phenotypes

Globoid cell leukodystrophy (GLD) is a rare neurodegenerative lysosomal storage disease caused by an inherited deficiency of β-galactocerebrosidase (GALC). GLD pathogenesis and therapeutic correction have been poorly studied in patient neural cells. Here, we investigated the impact of GALC deficienc...

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Detalles Bibliográficos
Autores principales: Mangiameli, Elisabeth, Cecchele, Anna, Morena, Francesco, Sanvito, Francesca, Matafora, Vittoria, Cattaneo, Angela, della Volpe, Lucrezia, Gnani, Daniela, Paulis, Marianna, Susani, Lucia, Martino, Sabata, Di Micco, Raffaella, Bachi, Angela, Gritti, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190599/
https://www.ncbi.nlm.nih.gov/pubmed/33989519
http://dx.doi.org/10.1016/j.stemcr.2021.04.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190599/
https://www.ncbi.nlm.nih.gov/pubmed/33989519
http://dx.doi.org/10.1016/j.stemcr.2021.04.011

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