{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE326nnn/GSE326402/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Homo sapiens"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE326402"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Variants in PATL1 can cause intellectual disability in humans revealed by modeling in Drosophila and C. Elegans","description":"P-bodies are dynamic, membrane-less organelles that function in mRNA metabolism that are involved in mRNA decay, storage, and translational repression. Here we introduce a new variant of the P-body protein encoding gene; PATL1, identified in an ID patient.","dates":{"publication":"2026/04/10"},"accession":"GSE326402","cross_references":{"GSM":["GSM9630464","GSM9630463","GSM9630468","GSM9630467","GSM9630466","GSM9630465"],"GPL":["29480"],"GSE":["326402"],"taxon":["Homo sapiens"]}}