Publication: Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
dc.contributor.author | Yücel-Yılmaz, D | |
dc.contributor.author | Yücesan, Emrah | |
dc.contributor.author | Yalnızoğlu, D | |
dc.contributor.author | Oğuz, KK | |
dc.contributor.author | Sağıroğlu, MŞ | |
dc.contributor.author | Özbek, U | |
dc.contributor.author | Serdaroğlu, E | |
dc.contributor.author | Bilgiç, B | |
dc.contributor.author | Erdem, S | |
dc.contributor.author | İşeri, SAU | |
dc.contributor.author | Hanağası, H | |
dc.contributor.author | Gürvit, H | |
dc.contributor.author | Özgül, RK | |
dc.contributor.author | Dursun, A | |
dc.contributor.institutionauthor | YÜCESAN, EMRAH | |
dc.date.accessioned | 2020-01-14T20:59:33Z | |
dc.date.available | 2020-01-14T20:59:33Z | |
dc.date.issued | 2018-06-01T00:00:00Z | |
dc.description.sponsorship | Türkiye Bilimsel Ve Teknolojik Araştırma Kurumu ( Tübitak ) | |
dc.description.sponsorship | İstanbul Üniversitesi | |
dc.identifier.citation | Yücel-Yılmaz D., Yücesan E., Yalnızoğlu D., Oğuz K., Sağıroğlu M., Özbek U., Serdaroğlu E., Bilgiç B., Erdem S., İşeri S., et al., -Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.-, Brain & development, cilt.40, ss.458-464, 2018 | |
dc.identifier.doi | 10.1016/j.braindev.2018.02.013 | |
dc.identifier.scopus | 85043456160 | |
dc.identifier.uri | https://openaccess.bezmialem.edu.tr/handle/20.500.12645/12732 | |
dc.identifier.wos | WOS:000433997300003 | |
dc.title | Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span. | |
dc.type | Article | |
dspace.entity.type | Publication | |
local.avesis.id | 2bd94994-4370-4dbf-b184-df6e4ea8595d | |
local.indexed.at | WOS | |
local.indexed.at | Scopus | |
local.publication.isinternational | 1 | |
relation.isAuthorOfPublication | 9ea2b80f-531b-49a7-83ef-723bfd8584b2 | |
relation.isAuthorOfPublication.latestForDiscovery | 9ea2b80f-531b-49a7-83ef-723bfd8584b2 |