Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes

Altuntas, CansuUzunhan, Tugce AksuErturk, BirayPetmezci, Mey TalipCakar, Nafiye EmelNoyan, BilgeLhsan Dokcu, Ali2024-05-192024-05-1920240303-84671872-6968https://doi.org10.1016/j.clineuro.2023.107893https://hdl.handle.net/20.500.12713/5365[Abstract Not Available]eninfo:eu-repo/semantics/closedAccessMngie SyndromeMitochondrial Dna Depletion SyndromeGastroparesisEncephalopathyResponse to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypesEditorial23637455189WOS:0011703627000012-s2.0-85184150718N/A10.1016/j.clineuro.2023.107893Q2