<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(11)</volume><submitter>Zeviani M</submitter><journal>European journal of human genetics : EJHG</journal><pagination>1593-1594</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8560914</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A de novo mutation in mitochondrial ATPsynthase subunit α causes a life threatening disease in neonates which heals in infancy.</pubmed_title><pmcid>PMC8560914</pmcid><pubmed_authors>Zeviani M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A de novo mutation in mitochondrial ATPsynthase subunit α causes a life threatening disease in neonates which heals in infancy.</name><description/><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-04T22:34:06.783Z</modification><creation>2025-02-19T03:24:01.49Z</creation></dates><accession>S-EPMC8560914</accession><cross_references><pubmed>34531511</pubmed><doi>10.1038/s41431-021-00965-z</doi></cross_references></HashMap>