A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delay

Wolfram syndrome (WS) is an ultra-rare progressive neurodegenerative disorder defined by early-onset diabetes mellitus and optic atrophy. The majority of patients harbour recessive mutations in the WFS1 gene, which encodes for Wolframin, a transmembrane endoplasmic reticulum protein. There is limite...

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Detalles Bibliográficos
Autores principales: Cairns, G., Burté, F., Price, R., O’Connor, E., Toms, M., Mishra, R., Moosajee, M., Pyle, A., Sayer, J. A., Yu-Wai-Man, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516871/
https://www.ncbi.nlm.nih.gov/pubmed/34650143
http://dx.doi.org/10.1038/s41598-021-99781-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516871/
https://www.ncbi.nlm.nih.gov/pubmed/34650143
http://dx.doi.org/10.1038/s41598-021-99781-0

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