Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleReply to the letter: "Is the variant m.9176T>C in MT‐ATP6 truly responsibly for Leigh syndrome?".AuthorsIchikawa, KazushiSubjectsGENETIC mutation; MITOCHONDRIAL pathology; LEIGH disease; PHENOTYPES; OCULOMOTOR paralysisPublicationPediatrics International, 2021, Vol 63, Issue 2, p240ISSN1328-8067Publication typeLetter to the EditorDOI10.1111/ped.14519