<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>205(3)</volume><submitter/><journal>The Journal of experimental medicine</journal><pagination>737-737</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2275393</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis</pubmed_title><pmcid>PMC2275393</pmcid></additional><is_claimable>false</is_claimable><name>Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis</name><description/><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Mar</publication><modification>2024-10-18T00:40:26.798Z</modification><creation>2024-10-18T00:40:26.798Z</creation></dates><accession>S-EPMC2275393</accession><cross_references/></HashMap>