FBXO7 mutation: Phenotypic variability from chorea to early-onset asymmetric parkinsonism within a family

dc.contributor.author	Gunel, M.
dc.contributor.author	Hanagasi, Haşmet Ayhan
dc.contributor.author	Bilguvar, K.
dc.contributor.author	Basak, A. N.
dc.contributor.author	Ertan, S.
dc.contributor.author	Gunduz, A.
dc.contributor.author	Eken, A. Gundogdu
dc.date.accessioned	2021-03-03T17:07:57Z
dc.date.available	2021-03-03T17:07:57Z
dc.identifier.citation	Gunduz A., Eken A. G. , Bilguvar K., Gunel M., Basak A. N. , Hanagasi H. A. , Ertan S., "FBXO7 mutation: Phenotypic variability from chorea to early-onset asymmetric parkinsonism within a family", MOVEMENT DISORDERS, cilt.28, 2013
dc.identifier.issn	0885-3185
dc.identifier.other	vv_1032021
dc.identifier.other	av_481bd19f-b824-4ea1-a61b-79eccc4b4e18
dc.identifier.uri	http://hdl.handle.net/20.500.12627/51996
dc.language.iso	eng
dc.subject	Dahili Tıp Bilimleri
dc.subject	Nöroloji
dc.subject	Tıp
dc.subject	Sağlık Bilimleri
dc.subject	Klinik Tıp (MED)
dc.subject	Klinik Tıp
dc.subject	KLİNİK NEUROLOJİ
dc.title	FBXO7 mutation: Phenotypic variability from chorea to early-onset asymmetric parkinsonism within a family
dc.type	Makale
dc.relation.journal	MOVEMENT DISORDERS
dc.contributor.department	, ,
dc.identifier.volume	28
dc.contributor.firstauthorID	1044444

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