Multiple Retinal Anomalies in Wfs1-Deficient Mice

Background: Wolfram syndrome (WFS, OMIM: #222300) is an ultrarare autosomal recessive disorder characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy and deafness. It has been reported that the average retinal thickness in WFS patients decreases with the progression of the disea...

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Detalles Bibliográficos
Autores principales: Waszczykowska, Arleta, Zmysłowska, Agnieszka, Braun, Marcin, Ivask, Marilin, Koks, Sulev, Jurowski, Piotr, Młynarski, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555979/
https://www.ncbi.nlm.nih.gov/pubmed/32824898
http://dx.doi.org/10.3390/diagnostics10090607

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555979/
https://www.ncbi.nlm.nih.gov/pubmed/32824898
http://dx.doi.org/10.3390/diagnostics10090607

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