A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study

Vodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Pusenjak, Marusa Skrjanec; Hodzic, Alenka; Miljanovic, Olivera; Peterlin, Borut; Writzl, Karin

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eNauka > Results > A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study

Title:	A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study
Authors:	Vodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Pusenjak, Marusa Skrjanec; Hodzic, Alenka; Miljanovic, Olivera; Peterlin, Borut; Writzl, Karin;
Issue Date:	2024
Publication:	EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN:	1018-4813 European Journal of Human Genetics Search Idenfier
Type:	Conference Paper
Collation:	vol. 32 str. 1390-1390
WoS-ID:	001407868902013
URI:	https://enauka.gov.rs/handle/123456789/974835
Project:	[P3-0326]
Metadata source:	(Preuzeto iz Nasi u WoS)
M-category:	Mp. category will be shown later

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