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Could the D614G substitution in the SARS-CoV-2 spike (S) protein be associated with higher COVID-19 mortality?
Eaaswarkhanth, Muthukrishnan; Al Madhoun, Ashraf; Al-Mulla, Fahd.
  • Eaaswarkhanth M; Department of Genetics and Bioinformatics, Dasman Diabetes Institute, Kuwait City, Kuwait.
  • Al Madhoun A; Department of Genetics and Bioinformatics, Dasman Diabetes Institute, Kuwait City, Kuwait.
  • Al-Mulla F; Department of Genetics and Bioinformatics, Dasman Diabetes Institute, Kuwait City, Kuwait. Electronic address: fahd.almulla@dasmaninstitute.org.
Int J Infect Dis ; 96: 459-460, 2020 Jul.
Article in English | MEDLINE | ID: covidwho-361379
ABSTRACT
The increasing number of deaths due to the COVID-19 pandemic has raised serious global concerns. Increased testing capacity and ample intensive care availability could explain lower mortality in some countries compared to others. Nevertheless, it is also plausible that the SARS-CoV-2 mutations giving rise to different phylogenetic clades are responsible for the apparent death rate disparities around the world. Current research literature linking the genetic make-up of SARS-CoV-2 with fatalities is lacking. Here, we suggest that this disparity in fatality rates may be attributed to SARS-CoV-2 evolving mutations and urge the international community to begin addressing the phylogenetic clade classification of SARS-CoV-2 in relation to clinical outcomes.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Spike Glycoprotein, Coronavirus / Betacoronavirus Type of study: Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2020 Document Type: Article Affiliation country: J.ijid.2020.05.071

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Spike Glycoprotein, Coronavirus / Betacoronavirus Type of study: Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Int J Infect Dis Journal subject: Communicable Diseases Year: 2020 Document Type: Article Affiliation country: J.ijid.2020.05.071