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