Morphological, behavioral and cellular analyses revealed different phenotypes in Wolfram syndrome wfs1a and wfs1b zebrafish mutant lines

Wolfram syndrome (WS) is a rare genetic disease characterized by diabetes, optic atrophy and deafness. Patients die at 35 years of age, mainly from respiratory failure or dysphagia. Unfortunately, there is no treatment to block the progression of symptoms and there is an urgent need for adequate res...

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Detalles Bibliográficos
Autores principales: Crouzier, Lucie, Richard, Elodie M, Diez, Camille, Alzaeem, Hala, Denus, Morgane, Cubedo, Nicolas, Delaunay, Thomas, Glendenning, Emily, Baxendale, Sarah, Liévens, Jean-Charles, Whitfield, Tanya T, Maurice, Tangui, Delprat, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402244/
https://www.ncbi.nlm.nih.gov/pubmed/35325133
http://dx.doi.org/10.1093/hmg/ddac065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402244/
https://www.ncbi.nlm.nih.gov/pubmed/35325133
http://dx.doi.org/10.1093/hmg/ddac065

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