Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleIs the variant m.9176T > C in MT‐ATP6 truly responsibly for Leigh syndrome?AuthorsFinsterer, JosefSubjectsMITOCHONDRIAL pathology; GENETIC mutation; PHENOTYPES; LEIGH disease; CHRONIC progressive external opthalmoplegiaPublicationPediatrics International, 2020, Vol 62, Issue 10, p1217ISSN1328-8067Publication typeLetter to the EditorDOI10.1111/ped.14383