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Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.

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dc.contributor.authorYücel-Yılmaz, D
dc.contributor.authorYücesan, Emrah
dc.contributor.authorYalnızoğlu, D
dc.contributor.authorOğuz, KK
dc.contributor.authorSağıroğlu, MŞ
dc.contributor.authorÖzbek, U
dc.contributor.authorSerdaroğlu, E
dc.contributor.authorBilgiç, B
dc.contributor.authorErdem, S
dc.contributor.authorİşeri, SAU
dc.contributor.authorHanağası, H
dc.contributor.authorGürvit, H
dc.contributor.authorÖzgül, RK
dc.contributor.authorDursun, A
dc.contributor.institutionauthorYÜCESAN, EMRAH
dc.date.accessioned2020-01-14T20:59:33Z
dc.date.available2020-01-14T20:59:33Z
dc.date.issued2018-06-01T00:00:00Z
dc.description.sponsorshipTürkiye Bilimsel Ve Teknolojik Araştırma Kurumu ( Tübitak )
dc.description.sponsorshipİstanbul Üniversitesi
dc.identifier.citationYücel-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.doi10.1016/j.braindev.2018.02.013
dc.identifier.scopus85043456160
dc.identifier.urihttps://openaccess.bezmialem.edu.tr/handle/20.500.12645/12732
dc.identifier.wosWOS:000433997300003
dc.titleClinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.
dc.typeArticle
dspace.entity.typePublication
local.avesis.id2bd94994-4370-4dbf-b184-df6e4ea8595d
local.publication.isinternational1
relation.isAuthorOfPublication9ea2b80f-531b-49a7-83ef-723bfd8584b2
relation.isAuthorOfPublication.latestForDiscovery9ea2b80f-531b-49a7-83ef-723bfd8584b2
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