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Lysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions

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dc.contributor.authorGörükmez, Orhan
dc.contributor.authorTürkgenç, Burcu
dc.contributor.authorGürkan, Hakan
dc.contributor.buuauthorAliyeva, Lamiya
dc.contributor.buuauthorErdöl, Şahin
dc.contributor.buuauthorYaralı, Yasin
dc.contributor.buuauthorBaytan, Birol
dc.contributor.buuauthorSağlam, Halil
dc.contributor.buuauthorKılıç, Şebnem
dc.contributor.buuauthorTemel, Şehime G.
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.orcid0000-0003-0710-5422
dc.contributor.researcheridAAG-8385-2021
dc.contributor.researcheridC-7392-2019
dc.contributor.researcheridAAH-1658-2021
dc.date.accessioned2024-01-10T12:09:47Z
dc.date.available2024-01-10T12:09:47Z
dc.date.issued2018-08-30
dc.descriptionBu çalışma, 26-28, Nisan 2018 tarihlerinde Athens[Yunanistan]’da düzenlenen European Biotechnology Congress Kongresi‘nde bildiri olarak sunulmuştur.
dc.identifier.citationAliyeva, L. vd. (2018). ''Lysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions''. Journal of Biotechnology, 280(Supplement S), S20-S20.
dc.identifier.doi10.1016/j.jbiotec.2018.06.061
dc.identifier.eissn1873-4863
dc.identifier.endpageS20
dc.identifier.issn0168-1656
dc.identifier.issueSupplement S
dc.identifier.startpageS20
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0168165618302372?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/11452/38943
dc.identifier.volume280
dc.identifier.wos000454825900059
dc.indexed.wosSCIE
dc.indexed.wosCPCIS
dc.language.isoen
dc.publisherElsevier
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalJournal of Biotechnology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiotechnology & applied microbiology
dc.subject.wosBiotechnology & applied microbiology
dc.titleLysinuric protein intolerance and HOIP deficiency in a boy: SLCA7A and RNF31 gene disruptions
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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