<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA769606</full_dataset_link><long_description>clinical and genetic analysis of combined oxidative phosphorylation defificiency-10 caused by MTO1 mutation</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>WES identified variants of MTO1 gene</description><dates><last_updated>2024-05-11</last_updated><first_public>2024-05-11</first_public></dates><accession>PRJNA769606</accession><cross_references/></HashMap>