<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(15)</volume><submitter>Cali F</submitter><funding>5xmille</funding><funding>Italian Ministry of Health “Ricerca Corrente 2017–2023”</funding><journal>International journal of molecular sciences</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12347329</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ZNF496 as Candidate Gene for Neurodevelopmental Disorders: Identification of a Pathogenic De Novo Frameshift Variant</pubmed_title><pmcid>PMC12347329</pmcid><pubmed_authors>Saccone S</pubmed_authors><pubmed_authors>Galati Rando R</pubmed_authors><pubmed_authors>Failla P</pubmed_authors><pubmed_authors>Musumeci A</pubmed_authors><pubmed_authors>Federico C</pubmed_authors><pubmed_authors>Papa C</pubmed_authors><pubmed_authors>Virgillito M</pubmed_authors><pubmed_authors>Treccarichi S</pubmed_authors><pubmed_authors>Cali F</pubmed_authors><pubmed_authors>Vinci M</pubmed_authors></additional><is_claimable>false</is_claimable><name>ZNF496 as Candidate Gene for Neurodevelopmental Disorders: Identification of a Pathogenic De Novo Frameshift Variant</name><description/><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-04-08T15:48:48.514Z</modification><creation>2026-04-08T05:36:27.716Z</creation></dates><accession>S-EPMC12347329</accession><cross_references/></HashMap>