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Browsing by Author Ovaert, C.
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2006
A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?
Gutierrez-Roelens, I.
;
Roy, L. De
;
Ovaert, C.
;
Sluysmans, T.
;
Devriendt, K.
, et al
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