<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(6)</volume><submitter>Hisama FM</submitter><journal>European journal of human genetics : EJHG</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4795068</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical utility gene card for: Werner Syndrome--Update 2014.</pubmed_title><pmcid>PMC4795068</pmcid><pubmed_authors>Martin GM</pubmed_authors><pubmed_authors>Kubisch C</pubmed_authors><pubmed_authors>Hisama FM</pubmed_authors><pubmed_authors>Oshima J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical utility gene card for: Werner Syndrome--Update 2014.</name><description/><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2025-04-05T12:18:51.851Z</modification><creation>2025-04-05T12:18:51.851Z</creation></dates><accession>S-EPMC4795068</accession><cross_references><pubmed>25182132</pubmed><doi>10.1038/ejhg.2014.171</doi></cross_references></HashMap>