[PMID 28714988
] SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.
[PMID 28842783] Population genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severity.
[PMID 30662816] Antiviral Protection by IFITM3 In Vivo.
[PMID 33174121] Ethnic variation in risk genotypes based on single nucleotide polymorphisms (SNPs) of the interferon-inducible transmembrane 3 (IFITM3) gene, a susceptibility factor for pandemic 2009 H1N1 influenza A virus.
[PMID 33240681] The frequency of combined IFITM3 haplotype involving the reference alleles of both rs12252 and rs34481144 is in line with COVID-19 standardized mortality ratio of ethnic groups in England.
] SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.
