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

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dc.authoridUzunhan, Tuğçe Aksu/0000-0003-0596-2690
dc.authoridAltuntaş, Cansu/0000-0002-1161-5145
dc.authoridErturk, Biray/0000-0002-0348-6267
dc.authorwosidUzunhan, Tuğçe Aksu/AAN-4010-2020
dc.authorwosidÇakar, Nafiye Emel/JRX-4283-2023
dc.authorwosidAltuntaş, Cansu/AGV-9547-2022
dc.contributor.authorAltuntas, Cansu
dc.contributor.authorUzunhan, Tugce Aksu
dc.contributor.authorErturk, Biray
dc.contributor.authorPetmezci, Mey Talip
dc.contributor.authorCakar, Nafiye Emel
dc.contributor.authorNoyan, Bilge
dc.contributor.authorLhsan Dokcu, Ali
dc.date.accessioned2024-05-19T14:45:50Z
dc.date.available2024-05-19T14:45:50Z
dc.date.issued2024
dc.departmentİstinye Üniversitesien_US
dc.description.abstract[Abstract Not Available]en_US
dc.identifier.doi10.1016/j.clineuro.2023.107893
dc.identifier.issn0303-8467
dc.identifier.issn1872-6968
dc.identifier.pmid37455189en_US
dc.identifier.scopus2-s2.0-85184150718en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.urihttps://doi.org10.1016/j.clineuro.2023.107893
dc.identifier.urihttps://hdl.handle.net/20.500.12713/5365
dc.identifier.volume236en_US
dc.identifier.wosWOS:001170362700001en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofClinical Neurology and Neurosurgeryen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmz20240519_kaen_US
dc.subjectMngie Syndromeen_US
dc.subjectMitochondrial Dna Depletion Syndromeen_US
dc.subjectGastroparesisen_US
dc.subjectEncephalopathyen_US
dc.titleResponse to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypesen_US
dc.typeEditorialen_US

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