A Family of HHH Syndrome with a Novel Missense Mutation in SLC25A15 Gene

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dc.contributor.authorAbur, U.
dc.contributor.authorOgur, G.
dc.contributor.authorDogan, C.
dc.contributor.authorAydin, H. I.
dc.contributor.authorAltundag, E.
dc.contributor.authorCeylaner, S.
dc.contributor.orcIDhttps://orcid.org/0000-0001-7994-4394en_US
dc.contributor.researcherIDAHD-1839-2022en_US
dc.date.accessioned2023-05-12T13:23:37Z
dc.date.available2023-05-12T13:23:37Z
dc.date.issued2018
dc.identifier.endpage293en_US
dc.identifier.issn1018-4813en_US
dc.identifier.startpage293en_US
dc.identifier.urihttp://hdl.handle.net/11727/9040
dc.identifier.volume26en_US
dc.identifier.wos000489312602152en_US
dc.language.isoengen_US
dc.relation.journalEUROPEAN JOURNAL OF HUMAN GENETICSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA Family of HHH Syndrome with a Novel Missense Mutation in SLC25A15 Geneen_US
dc.typeconferenceObjecten_US

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