<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(3)</volume><submitter>Moon B</submitter><funding>Korea Centers for Disease Control and Prevention</funding><journal>Clinical and experimental pediatrics</journal><pagination>142-144</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9989718</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome with atypical brain involvement.</pubmed_title><pmcid>PMC9989718</pmcid><funding_grant_id>2021-ER0701-00</funding_grant_id><pubmed_authors>Son HJ</pubmed_authors><pubmed_authors>Kim SY</pubmed_authors><pubmed_authors>Kim KJ</pubmed_authors><pubmed_authors>Moon B</pubmed_authors><pubmed_authors>Kim HJ</pubmed_authors><pubmed_authors>Lim BC</pubmed_authors><pubmed_authors>Chae JH</pubmed_authors><pubmed_authors>Kim M</pubmed_authors><pubmed_authors>Cho JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome with atypical brain involvement.</name><description/><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-06-01T02:34:22.455Z</modification><creation>2025-06-01T02:34:22.455Z</creation></dates><accession>S-EPMC9989718</accession><cross_references><pubmed>36596744</pubmed><doi>10.3345/cep.2022.01144</doi></cross_references></HashMap>