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Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

dc.contributor.authorEhlayel, MS
dc.contributor.authorKaraca, E
dc.contributor.authorArtac, H
dc.contributor.authorBayram, Y
dc.contributor.authorAtik, MM
dc.contributor.authorEldomery, MK
dc.contributor.authorJolles, S
dc.contributor.authorFlatø, B
dc.contributor.authorBertuch, AA
dc.contributor.authorHu, J
dc.contributor.authorWalkiewicz, M
dc.contributor.authorYang, Y
dc.contributor.authorEng, CM
dc.contributor.authorBoerwinkle, E
dc.contributor.authorGibbs, RA
dc.contributor.authorShearer, WT
dc.contributor.authorLyle, R
dc.contributor.authorOrange, JS
dc.contributor.authorLupski, JR
dc.contributor.authorYesil, Gözde
dc.contributor.authorStray-Pedersen, A
dc.contributor.authorSorte, HS
dc.contributor.authorSamarakoon, P
dc.contributor.authorGambin, T
dc.contributor.authorChinn, IK
dc.contributor.authorCoban, Akdemir
dc.contributor.authorErichsen, HC
dc.contributor.authorGu, S
dc.contributor.authorHanson, IC
dc.contributor.authorZhang, VW
dc.contributor.authorWong, LJ
dc.contributor.authorForbes, LR
dc.contributor.authorYuan, B
dc.contributor.authorJhangiani, SN
dc.contributor.authorMuzny, DM
dc.contributor.authorRødningen, OK
dc.contributor.authorSheng, Y
dc.contributor.authorNicholas, SK
dc.contributor.authorNoroski, LM
dc.contributor.authorSeeborg, FO
dc.contributor.authorDavis, CM
dc.contributor.authorCanter, DL
dc.contributor.authorMace, EM
dc.contributor.authorVece, TJ
dc.contributor.authorAllen, CE
dc.contributor.authorAbhyankar, HA
dc.contributor.authorBoone, PM
dc.contributor.authorBeck, CR
dc.contributor.authorWiszniewski, W
dc.contributor.authorFevang, B
dc.contributor.authorAukrust, P
dc.contributor.authorTjønnfjord, GE
dc.contributor.authorGedde-Dahl, T
dc.contributor.authorHjorth-Hansen, H
dc.contributor.authorDybedal, I
dc.contributor.authorNordøy, I
dc.contributor.authorJørgensen, SF
dc.contributor.authorAbrahamsen, TG
dc.contributor.authorØverland, T
dc.contributor.authorBechensteen, AG
dc.contributor.authorSkogen, V
dc.contributor.authorOsnes, LTN
dc.contributor.authorKulseth, MA
dc.contributor.authorPrescott, TE
dc.contributor.authorRustad, CF
dc.contributor.authorHeimdal, KR
dc.contributor.authorBelmont, JW
dc.contributor.authorRider, NL
dc.contributor.authorChinen, J
dc.contributor.authorCao, TN
dc.contributor.authorSmith, EA
dc.contributor.authorCaldirola, MS
dc.contributor.authorBezrodnik, L
dc.contributor.authorLugo, Reyes
dc.contributor.authorEspinosa, Rosales
dc.contributor.authorGuerrero-Cursaru, ND
dc.contributor.authorPedroza, LA
dc.contributor.authorPoli, CM
dc.contributor.authorFranco, JL
dc.contributor.authorTrujillo, Vargas
dc.contributor.authorAldave, Becerra
dc.contributor.authorWright, N
dc.contributor.authorIssekutz, TB
dc.contributor.authorIssekutz, AC
dc.contributor.authorAbbott, J
dc.contributor.authorCaldwell, JW
dc.contributor.authorBayer, DK
dc.contributor.authorChan, AY
dc.contributor.authorAiuti, A
dc.contributor.authorCancrini, C
dc.contributor.authorHolmberg, E
dc.contributor.authorWest, C
dc.contributor.authorBurstedt, M
dc.date.accessioned2021-03-04T17:22:59Z
dc.date.available2021-03-04T17:22:59Z
dc.identifier.citationStray-Pedersen A., Sorte H., Samarakoon P., Gambin T., Chinn I., Coban A., Erichsen H., Forbes L., Gu S., Yuan B., et al., "Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.", The Journal of allergy and clinical immunology, cilt.139, ss.232-245, 2017
dc.identifier.issn0091-6749
dc.identifier.otherav_85d8886c-4d6c-41ed-a53e-232103b19aae
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/90987
dc.identifier.urihttps://doi.org/10.1016/j.jaci.2016.05.042
dc.language.isoeng
dc.titlePrimary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
dc.typeMakale
dc.relation.journalThe Journal of allergy and clinical immunology
dc.contributor.department, ,
dc.identifier.volume139
dc.identifier.startpage232
dc.identifier.endpage245
dc.contributor.firstauthorID1042871


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