Mapping brain networks in MPS I mice and their restoration following gene therapy

Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal disorder that causes syndromes characterized by physiological dysfunction in many organs and tissues. Despite the recognizable morphological and behavioral deficits associated with MPS I, neither the underlying alterations in functional...

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Detalles Bibliográficos
Autores principales: Zhu, Wei, Ou, Li, Zhang, Lin, Clark, Isaac H., Zhang, Ying, Zhu, Xiao-Hong, Whitley, Chester B., Hackett, Perry B., Low, Walter C., Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404260/
https://www.ncbi.nlm.nih.gov/pubmed/37543633
http://dx.doi.org/10.1038/s41598-023-39939-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404260/
https://www.ncbi.nlm.nih.gov/pubmed/37543633
http://dx.doi.org/10.1038/s41598-023-39939-0

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