Vision and sensorimotor defects associated with loss of Vps11 function in a zebrafish model of genetic leukoencephalopathy

Genetic Leukoencephalopathies (gLEs) are heritable white matter disorders that cause progressive neurological abnormalities. A founder mutation in the human endolysosomal trafficking protein VPS11 has been identified in Ashkenazi Jewish patients manifesting classic gLE symptoms of hypomyelination, d...

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Detalles Bibliográficos
Autores principales: Banerjee, Shreya, Ranspach, Lillian E., Luo, Xixia, Cianciolo, Lauren T., Fogerty, Joseph, Perkins, Brian D., Thummel, Ryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894412/
https://www.ncbi.nlm.nih.gov/pubmed/35241734
http://dx.doi.org/10.1038/s41598-022-07448-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894412/
https://www.ncbi.nlm.nih.gov/pubmed/35241734
http://dx.doi.org/10.1038/s41598-022-07448-1

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