<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>69(5)</volume><submitter>Yaoita H</submitter><journal>Journal of human genetics</journal><pagination>185</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11043029</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Correction: Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.</pubmed_title><pmcid>PMC11043029</pmcid><pubmed_authors>Abiko M</pubmed_authors><pubmed_authors>Kikuchi A</pubmed_authors><pubmed_authors>Kure S</pubmed_authors><pubmed_authors>Tamiya G</pubmed_authors><pubmed_authors>Ozawa A</pubmed_authors><pubmed_authors>Iwasawa S</pubmed_authors><pubmed_authors>Kawai E</pubmed_authors><pubmed_authors>Saijo N</pubmed_authors><pubmed_authors>Suzuki K</pubmed_authors><pubmed_authors>Yaoita H</pubmed_authors><pubmed_authors>Takayama J</pubmed_authors><pubmed_authors>Kimura M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Correction: Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.</name><description/><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-04-22T20:44:31.923Z</modification><creation>2025-04-06T03:15:08.181Z</creation></dates><accession>S-EPMC11043029</accession><cross_references><pubmed>38548934</pubmed><doi>10.1038/s10038-024-01245-6</doi></cross_references></HashMap>