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A Case Series of Adenosine Deaminase 2 Deficient Patients Emphasizing Treatment and Genotype-Phenotype Correlations

dc.contributor.authorBatu, ED
dc.contributor.authorKaradağ, O
dc.contributor.authorTaskıran, EZ
dc.contributor.authorKalyoncu, U
dc.contributor.authorAksentijevich, I
dc.contributor.authorAlikasifoglu, M
dc.contributor.authorOzen, Seza
dc.date.accessioned2019-12-10T11:10:02Z
dc.date.available2019-12-10T11:10:02Z
dc.date.issued2015
dc.identifier.issn1546-0096
dc.identifier.urihttps://doi.org/10.1186/1546-0096-13-S1-P62
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599973/
dc.identifier.urihttp://hdl.handle.net/11655/14794
dc.relation.isversionof10.1186/1546-0096-13-S1-P62
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleA Case Series of Adenosine Deaminase 2 Deficient Patients Emphasizing Treatment and Genotype-Phenotype Correlations
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalPediatric Rheumatology Online Journal
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume13
dc.identifier.issueSuppl 1
dc.identifier.startpageP62
dc.description.indexPubMed
dc.description.indexScopus


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