Neuroimaging evidence of deficient axon myelination in Wolfram syndrome

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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Bibliographic Details
Main Authors: Lugar, Heather M., Koller, Jonathan M., Rutlin, Jerrel, Marshall, Bess A., Kanekura, Kohsuke, Urano, Fumihiko, Bischoff, Allison N., Shimony, Joshua S., Hershey, Tamara
Format: Online
Language:English
Published: Nature Publishing Group 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758056/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758056/

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