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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...
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| Publicado no: | Diagnostics (Basel) |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | 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 |
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