Cerebellar structural, astrocytic, and neuronal abnormalities in the SMNΔ7 mouse model of spinal muscular atrophy

Spinalmuscular atrophy (SMA) is a neuromuscular disease that affects as many as 1 in 6000 individuals at birth, making it the leading genetic cause of infant mortality. A growing number of studies indicate that SMA is a multi‐system disease. The cerebellum has received little attention even though i...

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Detalles Bibliográficos
Autores principales: Cottam, Nicholas C., Bamfo, Tiffany, Harrington, Melissa A., Charvet, Christine J., Hekmatyar, Khan, Tulin, Nikita, Sun, Jianli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467044/
https://www.ncbi.nlm.nih.gov/pubmed/37218083
http://dx.doi.org/10.1111/bpa.13162

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467044/
https://www.ncbi.nlm.nih.gov/pubmed/37218083
http://dx.doi.org/10.1111/bpa.13162

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