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The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.

dc.contributor.authorBONIFATI, V
dc.contributor.authorBilgiç, Başar
dc.contributor.authorQUADRI, M
dc.contributor.authorHANAGASI, Haşmet Ayhan
dc.contributor.authorGULTEKIN, Mehmet Hamza
dc.contributor.authorSÜRMELI, R
dc.contributor.authorSÜNTER, G
dc.contributor.authorDOĞAN, T
dc.contributor.authorYALÇıN, AD
dc.contributor.authorELIBOL, B
dc.contributor.authorEMRE, M
dc.contributor.authorOLGIATI, S
dc.contributor.authorDOĞU, O
dc.contributor.authorTUFEKCIOGLU, Z
dc.contributor.authorDILER, Y
dc.contributor.authorSAKA, E
dc.contributor.authorKALEAGASI, H
dc.contributor.authorKUIPERS, D
dc.contributor.authorGRAAFLAND, J
dc.contributor.authorBREEDVELD, GJ
dc.date.accessioned2021-03-06T07:49:39Z
dc.date.available2021-03-06T07:49:39Z
dc.identifier.citationOLGIATI S., DOĞU O., TUFEKCIOGLU Z., DILER Y., SAKA E., GULTEKIN M. H. , KALEAGASI H., KUIPERS D., GRAAFLAND J., BREEDVELD G., et al., "The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.", Parkinsonism & related disorders, cilt.39, ss.64-70, 2017
dc.identifier.issn1353-8020
dc.identifier.othervv_1032021
dc.identifier.otherav_de1853bb-7082-4eb1-a2d9-fbb229b150cb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/146317
dc.identifier.urihttps://doi.org/10.1016/j.parkreldis.2017.03.012
dc.language.isoeng
dc.titleThe p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.
dc.typeMakale
dc.relation.journalParkinsonism & related disorders
dc.contributor.department, ,
dc.identifier.volume39
dc.identifier.startpage64
dc.identifier.endpage70
dc.contributor.firstauthorID178399


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