A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy

dc.contributor.author	Bayrak, Ayşe Evrim
dc.contributor.author	Ünaltuna, Nihan
dc.contributor.author	Bayrak, Fatih
dc.contributor.author	Kahveci, Gökhan
dc.contributor.author	Mutlu, Bülent
dc.date.accessioned	2022-02-18T11:22:49Z
dc.date.available	2022-02-18T11:22:49Z
dc.identifier.citation	Mutlu B., Bayrak A. E. , Bayrak F., Kahveci G., Ünaltuna N., "A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy", European Society of Cardiology Congress, Stockholm, İsveç, 3 - 07 Eylül 2005, ss.1270
dc.identifier.other	vv_1032021
dc.identifier.other	av_f1710668-b965-4fe9-8c30-8cc86c724335
dc.identifier.uri	http://hdl.handle.net/20.500.12627/181079
dc.language.iso	eng
dc.subject	Sağlık Bilimleri
dc.subject	Klinik Tıp (MED)
dc.title	A Novel Mutation in PRKAG2 Responsible for Familial Wolff-Parkinson-White Syndrome and Severe Cardiac Hypertrophy
dc.type	Bildiri
dc.contributor.department	, ,
dc.contributor.firstauthorID	3067188

Bu öğenin dosyaları:

Dosyalar	Boyut	Biçim	Göster
Bu öğe ile ilişkili dosya yok.