<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Mehta S</submitter><journal>Journal of movement disorders</journal><pagination>107-109</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9978261</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder.</pubmed_title><pmcid>PMC9978261</pmcid><pubmed_authors>Lal V</pubmed_authors><pubmed_authors>Mehta S</pubmed_authors></additional><is_claimable>false</is_claimable><name>DHDDS Mutation: A Rare Cause of Refractory Epilepsy and Hyperkinetic Movement Disorder.</name><description/><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-22T21:47:58.074Z</modification><creation>2025-04-06T03:43:15.018Z</creation></dates><accession>S-EPMC9978261</accession><cross_references><pubmed>36628425</pubmed><doi>10.14802/jmd.22154</doi></cross_references></HashMap>