1. Açık Erişim@BUU
  2. İndeksli Yayınlar
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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29279
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dc.contributor.authorMorgan, Neil-
dc.contributor.authorWestaway, Shawn K.-
dc.contributor.authorMorton, Jenny-
dc.contributor.authorGregory, Allison-
dc.contributor.authorGissen, Paul-
dc.contributor.authorSonek, S.-
dc.contributor.authorCoryell, Jessi L.-
dc.contributor.authorCanham, N.-
dc.contributor.authorNardocci, Nardo-
dc.contributor.authorZorzi, Giovanna-
dc.contributor.authorPasha, Shanaz-
dc.contributor.authorRodriguez, D.-
dc.contributor.authorDesguerre, Isabelle-
dc.contributor.authorMubaidin, A.-
dc.contributor.authorBertini, Enrico-
dc.contributor.authorTrembath, Richard C.-
dc.contributor.authorSimonati, A.-
dc.contributor.authorSchanen, Carolyn-
dc.contributor.authorJohnson, Colin A.-
dc.contributor.authorLevinson, B.-
dc.contributor.authorWoods, Christopherg-
dc.contributor.authorWilmot, Brett-
dc.contributor.authorKramer, P.-
dc.contributor.authorGitschier, J.-
dc.contributor.authorHayflick, Susan J.-
dc.contributor.authorMaher, E. R.-
dc.date.accessioned2022-10-31T12:52:15Z-
dc.date.available2022-10-31T12:52:15Z-
dc.date.issued2006-09-
dc.identifier.citationMorgan, N. vd. (2006). ''The calcium-independent phospholipase A2 gene, PLA2G6, is mutated in a spectrum of childhood neurodegenerative disorders with high brain iron''. Journal of medical genetics, 43(Supplement 1), S27-S27.en_US
dc.identifier.issn0022-2593-
dc.identifier.urihttp://hdl.handle.net/11452/29279-
dc.language.isoenen_US
dc.publisherBmj Publishing Groupen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGenetics & heredityen_US
dc.titleThe calcium-independent phospholipase A2 gene, PLA2G6, is mutated in a spectrum of childhood neurodegenerative disorders with high brain ironen_US
dc.typeMeeting Abstracten_US
dc.identifier.wos000240957800032tr_TR
dc.relation.publicationcategoryKonferans Öğesi - Uluslararasıtr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.identifier.startpageS27tr_TR
dc.identifier.endpageS27tr_TR
dc.identifier.volume43tr_TR
dc.identifier.issueSupplement 1en_US
dc.relation.journalJournal of medical geneticsen_US
dc.contributor.buuauthorCangül, H.-
dc.relation.collaborationYurt dışıtr_TR
dc.subject.wosGenetics & heredityen_US
dc.indexed.wosSCIEen_US
dc.indexed.wosCPCISen_US
dc.wos.quartileQ1en_US
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