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10.1021/acsinfecdis.1c00268

http://scihub22266oqcxt.onion/10.1021/acsinfecdis.1c00268
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34569778!ä!34569778

suck abstract from ncbi


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pmid34569778      ACS+Infect+Dis 2021 ; 7 (10): 2787-2800
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  • A Closer Look into FDA-EUA Approved Diagnostic Techniques of Covid-19 #MMPMID34569778
  • Oh H; Ahn H; Tripathi A
  • ACS Infect Dis 2021[Oct]; 7 (10): 2787-2800 PMID34569778show ga
  • 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.
  • |*COVID-19[MESH]
  • |COVID-19 Testing[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |SARS-CoV-2[MESH]
  • |United States[MESH]


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