Evidence for altered neurodevelopment and neurodegeneration in Wolfram syndrome using longitudinal morphometry

Wolfram syndrome is a rare disease caused by mutations in the WFS1 gene leading to symptoms in early to mid-childhood. Brain structural abnormalities are present even in young children, but it is not known when these abnormalities arise. Such information is critical in determining optimal outcome me...

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Detalles Bibliográficos
Autores principales: Lugar, Heather M., Koller, Jonathan M., Rutlin, Jerrel, Eisenstein, Sarah A., Neyman, Olga, Narayanan, Anagha, Chen, Ling, Shimony, Joshua S., Hershey, Tamara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461605/
https://www.ncbi.nlm.nih.gov/pubmed/30979932
http://dx.doi.org/10.1038/s41598-019-42447-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461605/
https://www.ncbi.nlm.nih.gov/pubmed/30979932
http://dx.doi.org/10.1038/s41598-019-42447-9

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