<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(6)</volume><submitter>Yun JW</submitter><journal>Haematologica</journal><pagination>e274-e276</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6545837</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hereditary platelet function disorder from &lt;i>RASGRP2&lt;/i> gene mutations encoding CalDAG-GEFI identified by whole-exome sequencing in a Korean woman with severe bleeding.</pubmed_title><pmcid>PMC6545837</pmcid><pubmed_authors>Choi CW</pubmed_authors><pubmed_authors>Jung CW</pubmed_authors><pubmed_authors>Kim SH</pubmed_authors><pubmed_authors>Oh SY</pubmed_authors><pubmed_authors>Lee KO</pubmed_authors><pubmed_authors>Kim HJ</pubmed_authors><pubmed_authors>Yun JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hereditary platelet function disorder from &lt;i>RASGRP2&lt;/i> gene mutations encoding CalDAG-GEFI identified by whole-exome sequencing in a Korean woman with severe bleeding.</name><description/><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-05-07T05:17:03.634Z</modification><creation>2025-04-05T16:24:09.288Z</creation></dates><accession>S-EPMC6545837</accession><cross_references><pubmed>30846498</pubmed><doi>10.3324/haematol.2019.218487</doi></cross_references></HashMap>