Analysis of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome

Petitprez, S; Jespersen, T; Pruvot, E; Keller, D I; Corbaz, C; Schläpfer, J; Abriel, H; Kucera, J P (2008). Analysis of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome. Cardiovascular research, 78(3), pp. 494-504. Oxford: Oxford University Press 10.1093/cvr/cvn023

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Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Ionenkanalkrankheiten
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Ionenkanalkrankheiten

04 Faculty of Medicine > School of Dental Medicine > Department of Periodontology
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR)
04 Faculty of Medicine > Pre-clinic Human Medicine > Institute of Physiology

UniBE Contributor:

Petitprez, Séverine; Keller, Daniel; Abriel, Hugues and Kucera, Jan

ISSN:

0008-6363

Publisher:

Oxford University Press

Language:

English

Submitter:

Eveline Carmen Schuler

Date Deposited:

04 Oct 2013 15:04

Last Modified:

27 Apr 2018 08:32

Publisher DOI:

10.1093/cvr/cvn023

Web of Science ID:

000256738000013

BORIS DOI:

10.7892/boris.27623

URI:

https://boris.unibe.ch/id/eprint/27623 (FactScience: 109339)

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