Congenital analbuminemia in unrelated algerian and Turkish families is caused by the same molecular defect in the albumin gene
| dc.contributor.author | Caridi, Gianluca | |
| dc.contributor.author | Maout, Abdelbasset | |
| dc.contributor.author | Artan, Reha | |
| dc.contributor.author | Campagnoli, Monica | |
| dc.contributor.author | Lugani, Francesca | |
| dc.contributor.author | El Amine Abada, Mohamed | |
| dc.contributor.author | Sayar, Ersin | |
| dc.contributor.author | Galliano, Monica | |
| dc.contributor.author | Minchiotti, Lorenzo | |
| dc.date.accessioned | 2021-02-19T21:20:47Z | |
| dc.date.available | 2021-02-19T21:20:47Z | |
| dc.date.issued | 2018 | |
| dc.department | ALKÜ | |
| dc.description.abstract | [No abstract available] | |
| dc.description.sponsorship | Compagnia di San Paolo: ROL9849 | |
| dc.description.sponsorship | G.C. and F.L are supported by a grant from “Compagnia di San Paolo” (ROL9849). | |
| dc.identifier.doi | 10.3343/alm.2018.38.2.185 | |
| dc.identifier.endpage | 188 | en_US |
| dc.identifier.issn | 2234-3806 | |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.pmid | 29214768 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 185 | en_US |
| dc.identifier.uri | https://doi.org/10.3343/alm.2018.38.2.185 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12868/679 | |
| dc.identifier.volume | 38 | en_US |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.institutionauthor | 0-belirlenecek | |
| dc.language.iso | en | |
| dc.publisher | Seoul National University, Institute for Cognitive Science | |
| dc.relation.ispartof | Annals of Laboratory Medicine | |
| dc.relation.publicationcategory | Diğer | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.title | Congenital analbuminemia in unrelated algerian and Turkish families is caused by the same molecular defect in the albumin gene | |
| dc.type | Letter |
