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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Diagnostics (Basel) |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
MDPI
2020
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7555979/ https://ncbi.nlm.nih.gov/pubmed/32824898 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics10090607 |
| Tagiau: |
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