{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["34(3)"],"submitter":["Shirodkar AN"],"funding":["DBT/Wellcome Trust India Alliance","Wellcome Trust"],"journal":["Clinical dysmorphology"],"pagination":["102-106"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7617595"],"repository":["biostudies-literature"],"pubmed_title":["Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family."],"pmcid":["PMC7617595"],"funding_grant_id":["IA/CRC/20/1/600002"],"pubmed_authors":["Periyasamy R","Shukla A","Bhat V","Shirodkar AN","Akhil KA","Shah H"],"additional_accession":[]},"is_claimable":false,"name":"Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family.","description":null,"dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jul","modification":"2026-05-22T03:15:37.578Z","creation":"2026-05-22T03:08:34.483Z"},"accession":"S-EPMC7617595","cross_references":{"pubmed":["40073198"],"doi":["10.1097/mcd.0000000000000520","10.1097/MCD.0000000000000520"]}}