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Biomolecules ; 13(1)2023 01 09.
Article in English | MEDLINE | ID: mdl-36671517

ABSTRACT

Several studies have identified rare and common genetic variants associated with severe COVID-19, but no study has reported genetic determinants as predisposition factors for neurological complications. In this report, we identified rare/unique structural variants (SVs) implicated in neurological functions in two individuals with neurological manifestations of COVID-19. This report highlights the possible genetic link to the neurological symptoms with COVID-19 and calls for a collective effort to study these cohorts for a possible genetic linkage.


Subject(s)
COVID-19 , Nervous System Diseases , Humans , COVID-19/complications , COVID-19/genetics , Genetic Predisposition to Disease , Nervous System Diseases/genetics , Genotype
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