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dc.contributor.authorCaridi, Gianluca
dc.contributor.authorMaout, Abdelbasset
dc.contributor.authorArtan, Reha
dc.contributor.authorCampagnoli, Monica
dc.contributor.authorLugani, Francesca
dc.contributor.authorEl Amine Abada, Mohamed
dc.contributor.authorSayar, Ersin
dc.contributor.authorGalliano, Monica
dc.contributor.authorMinchiotti, Lorenzo
dc.date.accessioned2021-02-19T21:20:47Z
dc.date.available2021-02-19T21:20:47Z
dc.date.issued2018
dc.identifier.issn2234-3806
dc.identifier.urihttps://doi.org/10.3343/alm.2018.38.2.185
dc.identifier.urihttps://hdl.handle.net/20.500.12868/679
dc.descriptionPubMed: 29214768en_US
dc.description.abstract[No abstract available]en_US
dc.description.sponsorshipCompagnia di San Paolo: ROL9849en_US
dc.description.sponsorshipG.C. and F.L are supported by a grant from “Compagnia di San Paolo” (ROL9849).en_US
dc.language.isoengen_US
dc.publisherSeoul National University, Institute for Cognitive Scienceen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleCongenital analbuminemia in unrelated algerian and Turkish families is caused by the same molecular defect in the albumin geneen_US
dc.typeletteren_US
dc.contributor.departmentALKÜen_US
dc.contributor.institutionauthor0-belirlenecek
dc.identifier.doi10.3343/alm.2018.38.2.185
dc.identifier.volume38en_US
dc.identifier.issue2en_US
dc.identifier.startpage185en_US
dc.identifier.endpage188en_US
dc.relation.journalAnnals of Laboratory Medicineen_US
dc.relation.publicationcategoryDiğeren_US


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