Novel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme q10 deficiency

Görükmez, O.Görükmez, OrhanSağ, Şebnem ÖzemriErdöl, ŞahinSağlam, HalilYakut, T.2024-08-122024-08-122015-01-011015-8146https://hdl.handle.net/11452/43878eninfo:eu-repo/semantics/closedAccessQ(10) deficiencyMitochondrial encephalomyopathyScience & technologyLife sciences & biomedicineBiotechnology & applied microbiologyGenetics & heredityMedical ethicsMedicine, research & experimentalBiotechnology & applied microbiologyGenetics & heredityMedical ethicsResearch & experimental medicineNovel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme q10 deficiencyLetter000370466000016259262262