Multiple Retinal Anomalies in Wfs1-Deficient Mice.
Arleta WaszczykowskaAgnieszka ZmyslowskaMarcin BraunMarilin IvaskSulev KoksPiotr JurowskiWojciech MlynarskiPublished in: Diagnostics (Basel, Switzerland) (2020)
Wfs1KO mice retina with mutation in exon 8 present similar clinical features as patients with WFS in the form of reduced retinal thickness and neurodegeneration of the optic nerve. The presence of proliferative retinopathy observed in Wfs1KO mice requires further investigation.