Multiple Retinal Anomalies in Wfs1-Deficient Mice

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...

Full description

Bibliographic Details
Main Authors: Arleta Waszczykowska, Agnieszka Zmysłowska, Marcin Braun, Marilin Ivask, Sulev Koks, Piotr Jurowski, Wojciech Młynarski
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Diagnostics
Subjects:
Wolfram syndrome
wolframin
<i>Wfs1</i>
Wfs1KO mouse model
proliferative retinopathy
Online Access:https://www.mdpi.com/2075-4418/10/9/607

Internet

https://www.mdpi.com/2075-4418/10/9/607

Similar Items