A Homozygous IFNGR1 Mutation Revealed Rare Immunodeficiency Syndrome For A Patient Having Common Symptoms

Sunar, IlknurAkalin, Ayse BusraAkalin, IbrahimDemircioglu, FatihAlchalabi, MohammedDerin, ZeynepTavil, Betul2026-04-042026-04-0420241018-48131476-5438https://hdl.handle.net/11411/1075657th Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 01-04, 2024 -- Berlin, GERMANY[Abstract Not Available]eninfo:eu-repo/semantics/closedAccess[Keyword Not Available]A Homozygous IFNGR1 Mutation Revealed Rare Immunodeficiency Syndrome For A Patient Having Common SymptomsConference Object1032103232Q1WOS:001421430500632