<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/GSE317nnn/GSE317529/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Homo sapiens</species><gds_type> Expression profiling by high throughput sequencing</gds_type><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE317529</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy</name><description>This SuperSeries is composed of the SubSeries listed below.</description><dates><publication>2026/03/12</publication></dates><accession>GSE317529</accession><cross_references><GSM>GSM9420289</GSM><GSM>GSM9420288</GSM><GSM>GSM9420287</GSM><GSM>GSM9420286</GSM><GSM>GSM9420285</GSM><GSM>GSM9420284</GSM><GSM>GSM9420283</GSM><GSM>GSM9420293</GSM><GSM>GSM9420282</GSM><GSM>GSM9420292</GSM><GSM>GSM9420291</GSM><GSM>GSM9420290</GSM><GSM>GSM9428630</GSM><GSM>GSM9428628</GSM><GSM>GSM9428629</GSM><GPL>24676</GPL><GSE>317529</GSE><taxon>Homo sapiens</taxon><PMID>[41644016]</PMID></cross_references></HashMap>