Young-onset Parkinson's disease in two siblings with compound heterozygosity for two rare parkin mutations

dc.contributor.author	TUTUNCU, M.
dc.contributor.author	Poyraz, Burç Çağrı
dc.contributor.author	GUNDUZ, A.
dc.contributor.author	BASAK, A. N.
dc.contributor.author	APAYDIN, Hülya
dc.contributor.author	GUNDOGDU-EKEN, A.
dc.date.accessioned	2021-03-03T15:15:23Z
dc.date.available	2021-03-03T15:15:23Z
dc.identifier.citation	APAYDIN H., GUNDOGDU-EKEN A., GUNDUZ A., TUTUNCU M., Poyraz B. Ç. , BASAK A. N. , "Young-onset Parkinson's disease in two siblings with compound heterozygosity for two rare parkin mutations", 20th International Congress of Parkinson's Disease and Movement Disorders, Berlin, Almanya, 19 - 23 Haziran 2016, cilt.31
dc.identifier.other	vv_1032021
dc.identifier.other	av_3e12825a-13f2-4754-8007-e16d5f5f81e9
dc.identifier.uri	http://hdl.handle.net/20.500.12627/45593
dc.language.iso	eng
dc.subject	Sağlık Bilimleri
dc.subject	Dahili Tıp Bilimleri
dc.subject	Nöroloji
dc.subject	Klinik Tıp (MED)
dc.subject	Tıp
dc.subject	Klinik Tıp
dc.subject	KLİNİK NEUROLOJİ
dc.title	Young-onset Parkinson's disease in two siblings with compound heterozygosity for two rare parkin mutations
dc.type	Bildiri
dc.contributor.department	, ,
dc.identifier.volume	31
dc.contributor.firstauthorID	98753

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