Stray-Pedersen, AsbjorgSorte, Hanne SormoSamarakoon, PubuduGambin, TomaszChinn, Ivan K.Akdemir, Zeynep H. CobanErichsen, Hans ChristianForbes, Lisa R.Gu, ShenYuan, BoJhangiani, Shalini N.Muzny, Donna M.Rodningen, Olaug KristinSheng, YingNicholas, Sarah K.Noroski, Lenora M.Seeborg, Filiz O.Davis, Carla M.Canter, Debra L.Mace, Emily M.Vece, Timothy J.Allen, Carl E.Abhyankar, Harshal A.Boone, Philip M.Beck, Christine R.Wiszniewski, WojciechFevang, BorreAukrust, PalTjonnfjord, Geir E.Gedde-Dahl, TobiasHjorth-Hansen, HenrikDybedal, IngunnNordoy, IngvildJorgensen, Silje F.Abrahamsen, Tore G.Overland, TorsteinBechensteen, Anne GreteSkogen, VegardOsnes, Liv T. N.Kulseth, Mari AnnPrescott, Trine E.Rustad, Cecilie F.Heimdal, Ketil R.Belmont, John W.Rider, Nicholas L.Chinen, JavierCao, Tram N.Smith, Eric A.Soledad Caldirola, MariaBezrodnik, LilianaLugo Reyes, Saul OswaldoEspinosa Rosales, Francisco J.Guerrero-Cursaru, Nina DenissePedroza, Luis AlbertoPoli, Cecilia M.Franco, Jose L.Trujillo Vargas, Claudia M.Aldave Becerra, Juan CarlosWright, NicolaIssekutz, Thomas B.Issekutz, Andrew C.Abbott, JordanCaldwell, Jason W.Bayer, Diana K.Chan, Alice Y.Aiuti, AlessandroCancrini, CaterinaHolmberg, EvaWest, ChristinaBurstedt, MagnusKaraca, EnderYesil, GÖZDEArtac, HasibeBayram, YavuzAtik, Mehmed MusaEldomery, Mohammad K.Ehlayel, Mohammad S.Jolles, StephenFlato, BeritBertuch, Alison A.Hanson, I. CelineZhang, Victor W.Wong, Lee-JunHu, JianhongWalkiewicz, MagdalenaYang, YapingEng, Christine M.Boerwinkle, EricGibbs, Richard A.Shearer, William T.Lyle, RobertOrange, Jordan S.Lupski, James R.2019-11-172019-11-172017-01-01Stray-Pedersen A., Sorte H. S. , Samarakoon P., Gambin T., Chinn I. K. , Akdemir Z. H. C. , Erichsen H. C. , Forbes L. R. , Gu S., Yuan B., et al., -Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders-, JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, cilt.139, ss.232-245, 2017https://hdl.handle.net/20.500.12645/10396Background: Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous disorders thus far associated with mutations in more than 300 genes. The clinical phenotypes derived from distinct genotypes can overlap. Genetic etiology can be a prognostic indicator of disease severity and can influence treatment decisions. Objective: We sought to investigate the ability of whole-exome screening methods to detect disease-causing variants in patients with PIDDs.eninfo:eu-repo/semantics/openAccessArticle27577878trdizin