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Disease Causing Nature of Homozygous Missense, P.a523d, Alteration in the Perforin Gene

dc.authorscopusid 7005791514
dc.authorscopusid 7005245757
dc.authorscopusid 6701519928
dc.authorscopusid 8914207300
dc.authorscopusid 15070100200
dc.authorscopusid 6507853186
dc.authorscopusid 6507853186
dc.contributor.author Oner, A.F.
dc.contributor.author Okur, H.
dc.contributor.author Balta, G.
dc.contributor.author Unal, S.
dc.contributor.author Deger, I.
dc.contributor.author Akarsu, N.
dc.contributor.author Gurgey, A.
dc.date.accessioned 2025-05-10T17:06:46Z
dc.date.available 2025-05-10T17:06:46Z
dc.date.issued 2009
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Oner A.F., University, Faculty of Medicine, Division of Hematology, Van, Turkey; Okur H., Hacettepe University, Department of Pediatrics, Division of Pediatric Hematology, 06100 Sihhiye, Ankara, Turkey; Balta G., Hacettepe University, Department of Pediatrics, Division of Pediatric Hematology, 06100 Sihhiye, Ankara, Turkey; Unal S., Hacettepe University, Department of Pediatrics, Division of Pediatric Hematology, 06100 Sihhiye, Ankara, Turkey; Deger I., University, Faculty of Medicine, Division of Hematology, Van, Turkey; Akarsu N., Hacettepe University, Department of Pediatrics, Division of Pediatric Hematology, 06100 Sihhiye, Ankara, Turkey; Gurgey A., Hacettepe University, Department of Pediatrics, Division of Pediatric Hematology, 06100 Sihhiye, Ankara, Turkey en_US
dc.description.sponsorship TUBA; TÜBİTAK, (105S386, SBAG 3193) en_US
dc.identifier.doi 10.1016/j.leukres.2009.03.041
dc.identifier.endpage e153 en_US
dc.identifier.issn 0145-2126
dc.identifier.issue 9 en_US
dc.identifier.pmid 19464059
dc.identifier.scopus 2-s2.0-67549094643
dc.identifier.scopusquality Q3
dc.identifier.startpage e152 en_US
dc.identifier.uri https://doi.org/10.1016/j.leukres.2009.03.041
dc.identifier.uri https://hdl.handle.net/20.500.14720/6528
dc.identifier.volume 33 en_US
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.relation.ispartof Leukemia Research en_US
dc.relation.publicationcategory Diğer en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Disease Causing Nature of Homozygous Missense, P.a523d, Alteration in the Perforin Gene en_US
dc.type Letter en_US

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