{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["69(5)"],"submitter":["Yaoita H"],"journal":["Journal of human genetics"],"pagination":["185"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11043029"],"repository":["biostudies-literature"],"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."],"pmcid":["PMC11043029"],"pubmed_authors":["Abiko M","Kikuchi A","Kure S","Tamiya G","Ozawa A","Iwasawa S","Kawai E","Saijo N","Suzuki K","Yaoita H","Takayama J","Kimura M"],"additional_accession":[]},"is_claimable":false,"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.","description":null,"dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 May","modification":"2025-04-22T20:44:31.923Z","creation":"2025-04-06T03:15:08.181Z"},"accession":"S-EPMC11043029","cross_references":{"pubmed":["38548934"],"doi":["10.1038/s10038-024-01245-6"]}}