QuickView for IFNAR2;jsessionid=D8162E65A7636FD2044C30F4D635C40B;jsessionid=7BA41F0C2DF0F9F0334D09920E13798B;jsessionid=CDDF12A8552D8903835973712B64E16A;jsessionid=4C1DA45046D77047176410BBF3FA6749;jsessionid=1B8BC8E3CA78177C70799E83C1645FFF (gene)

1. Deleterious single nucleotide polymorphisms (SNPs) of human IFNAR2 gene facilitate COVID-19 severity…
2. IFNAR2 relevance in the clinical outcome of individuals with severe COVID-19.
3. Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 deficiency in the Arcti…
4. Loss-of-function mutations in IFNAR2 in COVID-19 severe infection susceptibility.
5. Null IFNAR1 and IFNAR2 alleles are surprisingly common in the Pacific and Arctic.

There were no clinical trials for IFNAR2;jsessionid=D8162E65A7636FD2044C30F4D635C40B;jsessionid=7BA41F0C2DF0F9F0334D09920E13798B;jsessionid=CDDF12A8552D8903835973712B64E16A;jsessionid=4C1DA45046D77047176410BBF3FA6749;jsessionid=1B8BC8E3CA78177C70799E83C1645FFF