A novel mutation in PRKAG2 responsible for familial Wolff-Parkinson-White syndrome and severe cardiac hypertrophy

dc.contributor.author	BAYRAK, F.
dc.contributor.author	BASARAN, Yusuf
dc.contributor.author	BAYRAK, E. Komurcu
dc.contributor.author	KAHVECI, G.
dc.contributor.author	Unaltuna, Nihan
dc.contributor.author	MUTLU, B.
dc.date.accessioned	2021-03-05T21:23:27Z
dc.date.available	2021-03-05T21:23:27Z
dc.identifier.citation	MUTLU B., BAYRAK E. K. , BAYRAK F., KAHVECI G., BASARAN Y., Unaltuna N., "A novel mutation in PRKAG2 responsible for familial Wolff-Parkinson-White syndrome and severe cardiac hypertrophy", 27th Congress of the European-Society-of-Cardiology, Stockholm, İsveç, 3 - 07 Eylül 2005, cilt.26, ss.198
dc.identifier.other	vv_1032021
dc.identifier.other	av_d8a8a274-269c-41cc-a686-35be5916a21f
dc.identifier.uri	http://hdl.handle.net/20.500.12627/142948
dc.language.iso	eng
dc.subject	Sağlık Bilimleri
dc.subject	Dahili Tıp Bilimleri
dc.subject	Kardiyoloji
dc.subject	Klinik Tıp (MED)
dc.subject	Tıp
dc.subject	Klinik Tıp
dc.subject	CARDIAC ve CARDIOVASCULAR SİSTEMLER
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.identifier.volume	26
dc.contributor.firstauthorID	28629

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