{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["12(3)"],"submitter":["Li Y"],"journal":["Molecular genetics & genomic medicine"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10912793"],"repository":["biostudies-literature"],"pubmed_title":["Clinical report and genetic analysis of rare premature infant nephronophthisis caused by biallelic TTC21B variants"],"pmcid":["PMC10912793"],"pubmed_authors":["Li Y","Dai L","Huang J","Zhang J","Mei Z","Xu H","Zhang R"],"additional_accession":[]},"is_claimable":false,"name":"Clinical report and genetic analysis of rare premature infant nephronophthisis caused by biallelic TTC21B variants","description":null,"dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Mar","modification":"2024-11-14T22:23:55.521Z","creation":"2024-11-14T22:23:55.521Z"},"accession":"S-EPMC10912793","cross_references":{}}