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- Q91661654 description "article scientifique publié en 2020" @default.
- Q91661654 description "artículu científicu espublizáu n'abril de 2020" @default.
- Q91661654 description "scientific article published on 07 April 2020" @default.
- Q91661654 description "wetenschappelijk artikel" @default.
- Q91661654 description "наукова стаття, опублікована 7 квітня 2020" @default.
- Q91661654 description "գիտական հոդված հրատարակված 2020 թվականի ապրիլի 7-ին" @default.
- Q91661654 name "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 name "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 type Item @default.
- Q91661654 label "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 label "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 prefLabel "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 prefLabel "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 P1433 Q91661654-F99575FC-66CB-43CC-8653-A3714D73F900 @default.
- Q91661654 P1476 Q91661654-5634A3C8-1D3C-43B1-BB92-E89D9D34FE0E @default.
- Q91661654 P2093 Q91661654-3430A36C-3A43-4096-98A4-1C827495F469 @default.
- Q91661654 P2093 Q91661654-66D86EF8-34A0-42F3-A628-3400C04E6FA8 @default.
- Q91661654 P2093 Q91661654-73C894B9-4833-4BB1-9AEF-C4464D09D4BA @default.
- Q91661654 P2093 Q91661654-9DA0FEFF-4E8C-4CF9-8C75-84985F694A73 @default.
- Q91661654 P2093 Q91661654-D413FBE2-9C0C-42DD-A160-A4DC3ED05BFF @default.
- Q91661654 P31 Q91661654-94C23B6D-2A50-4673-ABEB-A07109EDF42E @default.
- Q91661654 P356 Q91661654-47BE31DF-B288-4295-AC5F-3078E022092E @default.
- Q91661654 P50 Q91661654-3146F2CB-F97A-46FE-97F4-A0E080271C0E @default.
- Q91661654 P577 Q91661654-F6A12D0B-C2B2-4C12-A9B4-1926E25D91CF @default.
- Q91661654 P698 Q91661654-B273E23D-4808-41BC-AAD8-E019433C006E @default.
- Q91661654 P921 Q91661654-CBCDB85B-C72B-46BA-970E-0B149091B99E @default.
- Q91661654 P356 AJMG.A.61590 @default.
- Q91661654 P698 32259399 @default.
- Q91661654 P1433 Q4744254 @default.
- Q91661654 P1476 "Expanding the clinical spectrum of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review" @default.
- Q91661654 P2093 "Ali Topak" @default.
- Q91661654 P2093 "Fatih S Ezgu" @default.
- Q91661654 P2093 "Mutlu U Yazıcı" @default.
- Q91661654 P2093 "Sevil Dorum" @default.
- Q91661654 P2093 "Turgay Coskun" @default.
- Q91661654 P31 Q13442814 @default.
- Q91661654 P356 "10.1002/AJMG.A.61590" @default.
- Q91661654 P50 Q88939423 @default.
- Q91661654 P577 "2020-04-07T00:00:00Z" @default.
- Q91661654 P698 "32259399" @default.
- Q91661654 P921 Q55783430 @default.