Metli, KubraZamani, AyseOzdemir, TahaYildirim, M. Selman2024-02-232024-02-2320211096-71921096-7206https://hdl.handle.net/20.500.12452/18173[Abstract Not Availabe]eninfo:eu-repo/semantics/closedAccess[Keyword Not Available]A rare homozygous microdeletion syndrome: hypotonia-cystinuria syndromeConference Object132S120S120Q2WOS:000639219800180Q2