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, Kucera, Jan

ISSN:

 0008-6363

Publisher:

 Oxford University Press

Language:

 English

Submitter:

 Eveline Carmen Schuler

Date Deposited:

 04 Oct 2013 15:04

Last Modified:

 05 Dec 2022 14:19

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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