<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Nan H</submitter><journal>Molecular genetics &amp; genomic medicine</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10915366</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Okur‐Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion</pubmed_title><pmcid>PMC10915366</pmcid><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Nan H</pubmed_authors><pubmed_authors>Jiang D</pubmed_authors><pubmed_authors>Chu M</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Okur‐Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion</name><description/><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-05-29T12:06:59.343Z</modification><creation>2026-04-08T04:48:44.34Z</creation></dates><accession>S-EPMC10915366</accession><cross_references/></HashMap>