<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE282nnn/GSE282281/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE282281</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single cell RNA seq profile of Control and EPM1 patient's derived ventral brain organoids as single genotype or as mosaic at 40 days</name><description>This study uses single-cell RNA sequencing (scRNA-seq) to explore the pathogenesis of progressive myoclonus epilepsy type 1 (EPM1) in cerebral organoids derived from patient cells. The analysis reveals a shift in progenitor fate toward dorsal neuron identities and a reduction in inhibitory interneurons, disrupting the excitatory/inhibitory balance and increasing electrophysiological activity.</description><dates><publication>2026/09/01</publication></dates><accession>GSE282281</accession><cross_references><GSM>GSM8640489</GSM><GSM>GSM8640496</GSM><GSM>GSM8640494</GSM><GSM>GSM8640495</GSM><GSM>GSM8640492</GSM><GSM>GSM8640493</GSM><GSM>GSM8640490</GSM><GSM>GSM8640491</GSM><GPL>24676</GPL><GSE>282281</GSE><taxon>Homo sapiens</taxon><PMID>[42685196]</PMID></cross_references></HashMap>