Neuroimaging evidence of deficient axon myelination in Wolfram syndrome

Wolfram syndrome is a rare autosomal recessive genetic disease characterized by insulin dependent diabetes and vision, hearing and brain abnormalities which generally emerge in childhood. Mutations in the WFS1 gene predispose cells to endoplasmic reticulum stress-mediated apoptosis and may induce my...

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Detalles Bibliográficos
Autores principales: Lugar, Heather M., Koller, Jonathan M., Rutlin, Jerrel, Marshall, Bess A., Kanekura, Kohsuke, Urano, Fumihiko, Bischoff, Allison N., Shimony, Joshua S., Hershey, Tamara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758056/
https://www.ncbi.nlm.nih.gov/pubmed/26888576
http://dx.doi.org/10.1038/srep21167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758056/
https://www.ncbi.nlm.nih.gov/pubmed/26888576
http://dx.doi.org/10.1038/srep21167

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