{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["272(2)"],"submitter":["Sabbagh Q"],"journal":["Journal of neurology"],"pagination":["154"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11742001"],"repository":["biostudies-literature"],"pubmed_title":["AP4B1 hypomorphic variants cause autosomal recessive adult-onset ataxia."],"pmcid":["PMC11742001"],"pubmed_authors":["Ramond F","Sabbagh Q","Angelini C","Fluchere F","Pointaux M","Lesca G","Benkirane M","Hersent C","Castrioto A","Deberge L","Goizet C","Poblete NH","Larrieu L","Koenig M"],"additional_accession":[]},"is_claimable":false,"name":"AP4B1 hypomorphic variants cause autosomal recessive adult-onset ataxia.","description":null,"dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jan","modification":"2026-04-14T03:18:45.268Z","creation":"2025-04-19T13:40:49.602Z"},"accession":"S-EPMC11742001","cross_references":{"pubmed":["39821477"],"doi":["10.1007/s00415-025-12889-5"]}}