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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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Foilsithe in:iScience
Main Authors: Velez, Gabriel, Mahajan, Vinit B.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Elsevier 2020
Ábhair:
Rochtain Ar Líne: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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