Atli, EnginGurkan, HakanUlusal, SelmaKaral, YaseminAtli, Emine I.Tozkir, Hilmi2024-06-122024-06-1220180962-88271473-5717https://doi.org/10.1097/MCD.0000000000000204https://hdl.handle.net/20.500.14551/25165[Abstract Not Available]en10.1097/MCD.0000000000000204info:eu-repo/semantics/closedAccessMental-RetardationDeafnessIdentification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndromeArticle27113Q4WOS:0004181310000012-s2.0-8503823263329176366Q3