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