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C19orf12 p.Thr11Met mutation is frequent among adult Turkish patients with MPAN

dc.contributor.authorBreedveld, G.
dc.contributor.authorKuipers, D.
dc.contributor.authorGraafland, J.
dc.contributor.authorSurmeli, R.
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorBonifati, V.
dc.contributor.authorEmre, M.
dc.contributor.authorElibol, B.
dc.contributor.authorBilgic, B.
dc.contributor.authorYalcin, D.
dc.contributor.authorDogan, T.
dc.contributor.authorSunter, G.
dc.contributor.authorQuadri, M.
dc.contributor.authorOlgiati, S.
dc.contributor.authorDogu, O.
dc.contributor.authorTufekcioglu, Z.
dc.contributor.authorDiler, Y.
dc.contributor.authorSaka, E.
dc.contributor.authorGultekin, M.
dc.contributor.authorKaleagasi, H.
dc.date.accessioned2021-03-05T11:46:51Z
dc.date.available2021-03-05T11:46:51Z
dc.identifier.citationQuadri M., Olgiati S., Dogu O., Tufekcioglu Z., Diler Y., Saka E., Gultekin M., Kaleagasi H., Kuipers D., Graafland J., et al., "C19orf12 p.Thr11Met mutation is frequent among adult Turkish patients with MPAN", 21st International Congress of Parkinson's Disease and Movement Disorders, Vancouver, Kanada, 4 - 08 Haziran 2017, cilt.32
dc.identifier.othervv_1032021
dc.identifier.otherav_a9dbb803-f063-4764-84b9-a47387d77336
dc.identifier.urihttp://hdl.handle.net/20.500.12627/113442
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.titleC19orf12 p.Thr11Met mutation is frequent among adult Turkish patients with MPAN
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume32
dc.contributor.firstauthorID1044318


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