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Clinical Features of the -Optineurin- Mutation in familial FTD and ALS

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dc.contributor.authorCikrikcili, Ugur
dc.contributor.authorDurmus, Hacer
dc.contributor.authorBasak, Nazli
dc.contributor.authorGunel, Murat
dc.contributor.authorGÜRVİT, İbrahim Hakan
dc.contributor.authorMatur, ZELİHA
dc.contributor.authorAkca Kalem, Sukriy
dc.contributor.authorSerdaroglu-Oflazer, Piraye
dc.contributor.authorDeymeer, Feza
dc.contributor.authorParman, Yesim
dc.contributor.institutionauthorMATUR, ZELİHA
dc.date.accessioned2022-01-13T21:00:20Z
dc.date.available2022-01-13T21:00:20Z
dc.date.issued2012-01-01T00:00:00Z
dc.identifier.urihttp://hdl.handle.net/20.500.12645/30178
dc.identifier.wosWOS:000308612400335
dc.subjectCikrikcili U., Durmus H., Basak N., Gunel M., GÜRVİT İ. H. , Matur Z., Akca Kalem S., Serdaroglu-Oflazer P., Deymeer F., Parman Y., -Clinical Features of the -Optineurin- Mutation in familial FTD and ALS-, 8th International Conference on Frontotemporal Dementias, Manchester, İngiltere, 5 - 07 Eylül 2012, cilt.33, ss.231
dc.titleClinical Features of the -Optineurin- Mutation in familial FTD and ALS
dc.typeConference Paper
dspace.entity.typePublication
local.avesis.idce6b23a9-b17d-4ac9-bd10-e8d09db47c0d
local.publication.isinternational1
relation.isAuthorOfPublication3c69fce6-5ba0-4838-9215-eae7a7125446
relation.isAuthorOfPublication.latestForDiscovery3c69fce6-5ba0-4838-9215-eae7a7125446
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