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dc.contributor.authorGUNEL, M
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorSESTAN, N
dc.contributor.authorLOUVI, A
dc.contributor.authorCAGLAYAN, Ayça Yeşim
dc.contributor.authorSGOURDOU, P
dc.contributor.authorMISHRA-GORUR, K
dc.contributor.authorSAOTOME, I
dc.contributor.authorHENAGARIU, O
dc.contributor.authorCAMPOS, C
dc.contributor.authorISHIGAME, K
dc.contributor.authorGIANNIKOU, K
dc.contributor.authorQUON, JL
dc.date.accessioned2021-03-03T18:18:05Z
dc.date.available2021-03-03T18:18:05Z
dc.identifier.citationSGOURDOU P., MISHRA-GORUR K., SAOTOME I., HENAGARIU O., Tuysuz B., CAMPOS C., ISHIGAME K., GIANNIKOU K., QUON J., SESTAN N., et al., "Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.", Scientific reports, cilt.7, ss.43708, 2017
dc.identifier.issn2045-2322
dc.identifier.othervv_1032021
dc.identifier.otherav_4e4dfc0c-1444-4dd8-873c-a49f9fb5060f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/55936
dc.identifier.urihttps://doi.org/10.1038/srep43708
dc.language.isoeng
dc.titleDisruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.
dc.typeMakale
dc.relation.journalScientific reports
dc.contributor.department, ,
dc.identifier.volume7
dc.identifier.startpage43708
dc.identifier.endpage43708
dc.contributor.firstauthorID123629


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