Progressive Myoclonic Epilepsy and NEU1 Mutation: A Different
Phenotypic Case

dc.contributor.author	Lehesjoki, Anna-Elina
dc.contributor.author	BEBEK, Nerses
dc.contributor.author	Guerses, C.
dc.contributor.author	Gokyigit, A.
dc.contributor.author	BAYKAN, Betül
dc.contributor.author	Vanli, Ebru
dc.contributor.author	UZUN, GUNES ALTIOKKA
dc.contributor.author	Matur, Zeliha
dc.contributor.author	Muana, Mikko
dc.date.accessioned	2021-03-04T18:23:43Z
dc.date.available	2021-03-04T18:23:43Z
dc.identifier.citation	Vanli E., UZUN G. A. , Matur Z., Muana M., BEBEK N., Guerses C., Lehesjoki A., Gokyigit A., BAYKAN B., "Progressive Myoclonic Epilepsy and NEU1 Mutation: A Different Phenotypic Case", Türk Nöroloji Dergisi, cilt.22, ss.84-87, 2016
dc.identifier.issn	0716-0852
dc.identifier.other	vv_1032021
dc.identifier.other	av_8a728487-6c03-449c-be35-7ad9568226dd
dc.identifier.uri	http://hdl.handle.net/20.500.12627/93847
dc.language.iso	tur
dc.subject	Tıp
dc.subject	Klinik Tıp (MED)
dc.subject	Sağlık Bilimleri
dc.title	Progressive Myoclonic Epilepsy and NEU1 Mutation: A Different Phenotypic Case
dc.type	Makale
dc.relation.journal	Türk Nöroloji Dergisi
dc.contributor.department	Diğer Kurumlar , ,
dc.identifier.volume	22
dc.identifier.startpage	84
dc.identifier.endpage	87
dc.contributor.firstauthorID	638452

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