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suck abstract from ncbi


10.1038/s41392-021-00736-8

http://scihub22266oqcxt.onion/10.1038/s41392-021-00736-8
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34545062!8450706!34545062
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suck abstract from ncbi

pmid34545062      Signal+Transduct+Target+Ther 2021 ; 6 (1): 344
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  • Human genetic basis of coronavirus disease 2019 #MMPMID34545062
  • Deng H; Yan X; Yuan L
  • Signal Transduct Target Ther 2021[Sep]; 6 (1): 344 PMID34545062show ga
  • Coronavirus disease 2019 (COVID-19) caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in considerable morbidity and mortality worldwide. COVID-19 incidence, severity, and mortality rates differ greatly between populations, genders, ABO blood groups, human leukocyte antigen (HLA) genotypes, ethnic groups, and geographic backgrounds. This highly heterogeneous SARS-CoV-2 infection is multifactorial. Host genetic factors such as variants in the angiotensin-converting enzyme gene (ACE), the angiotensin-converting enzyme 2 gene (ACE2), the transmembrane protease serine 2 gene (TMPRSS2), along with HLA genotype, and ABO blood group help to explain individual susceptibility, severity, and outcomes of COVID-19. This review is focused on COVID-19 clinical and viral characteristics, pathogenesis, and genetic findings, with particular attention on genetic diversity and variants. The human genetic basis could provide scientific bases for disease prediction and targeted therapy to address the COVID-19 scourge.
  • |ABO Blood-Group System/genetics[MESH]
  • |Angiotensin-Converting Enzyme 2/*genetics[MESH]
  • |COVID-19/epidemiology/*genetics/virology[MESH]
  • |Ethnicity/genetics[MESH]
  • |Female[MESH]
  • |Genotype[MESH]
  • |HLA Antigens/genetics[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Peptidyl-Dipeptidase A/*genetics[MESH]
  • |Risk Factors[MESH]
  • |SARS-CoV-2/*genetics/pathogenicity[MESH]


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