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Molecular Surgery: Proteomics of a Rare Genetic Disease Gives Insight into Common Causes of Blindness
Rare diseases are an emerging global health priority. Although individually rare, the prevalence of rare “orphan” diseases is high, affecting approximately 300 million people worldwide. Treatments for these conditions are often inadequate, leaving the disease to progress unabated. Here, we review th...
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| Izdano u: | iScience |
|---|---|
| Glavni autori: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7586135/ https://ncbi.nlm.nih.gov/pubmed/33134897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.isci.2020.101667 |
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