Characterization of the Expression of Vacuolar Protein Sorting 11 (Vps11) in Mammalian Oligodendrocytes

A founder mutation in human VPS11 (Vacuolar Protein Sorting 11) was recently linked to a genetic leukoencephalopathy in Ashkenazi Jews that presents with the classical features of white matter disorders of the central nervous system (CNS). The neurological deficits include hypomyelination, hypotonia...

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Detalles Bibliográficos
Autores principales: Skoff, Robert P., Bessert, Denise, Banerjee, Shreya, Luo, Xixia, Thummel, Ryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060772/
https://www.ncbi.nlm.nih.gov/pubmed/33874780
http://dx.doi.org/10.1177/17590914211009851

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060772/
https://www.ncbi.nlm.nih.gov/pubmed/33874780
http://dx.doi.org/10.1177/17590914211009851

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