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- W3201764237 abstract "The 2019 coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 virus, caused a worldwide pandemic in 2020 and is the most urgent health issue worldwide. In this review, we highlight the details of Food and Drug Administration-Emergency Use Authorizations approved diagnostics kits, focusing on the similarities and differences. It is essential to understand the currently available options and the advantages and disadvantages each provides to select the appropriate products that maximize the testing efficiency. We believe this work will provide a holistic evaluation of the current COVID-19 diagnostic resources, including variations across the countries, and guide developing novel diagnostic techniques to improve and optimize the current testing options." @default.
- W3201764237 created "2021-10-11" @default.
- W3201764237 creator A5033441436 @default.
- W3201764237 creator A5080169355 @default.
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- W3201764237 date "2021-09-27" @default.
- W3201764237 modified "2023-10-05" @default.
- W3201764237 title "A Closer Look into FDA-EUA Approved Diagnostic Techniques of Covid-19" @default.
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- W3201764237 doi "https://doi.org/10.1021/acsinfecdis.1c00268" @default.
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