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Cardiac electrophysiology
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Mutations in MYT1, encoding the...
Mutations in
MYT1
, encoding the myelin transcription factor 1, are a rare cause of OAVS.
Publié en June 2016
Journal of medical genetics
June 2016
Proarrhythmic remodelling of the right ventricle in a porcine model of repaired tetralogy of Fallot.
Journal of medical genetics
Previous publication
June 2016
Identification of Region-Specific Myocardial Gene Expression Patterns in a Chronic Swine Model of Repaired Tetralogy of Fallot.
Journal of medical genetics
Next publication
Authors
Lopez E
Berenguer M
Tingaud-Sequeira A
Marlin S
Toutain A
Denoyelle F
Picard A
Charron S
Mathieu G
de Belvalet H
Arveiler B
Babin PJ
Lacombe D
Rooryck C