La expresividad variable del síndrome de QT largo de una familia española se explica por la heterocigosis digénica en SCN5A y CACNA1C

Nieto-Marín, Paloma; Jiménez-Jáimez, Juan; Tinaquero, David; Alfayate, Silvia; Utrilla, Raquel G; Rodríguez Vázquez del Rey, María del Mar; Perin, Francesca; Sarquella-Brugada, Geòrgia; Monserrat, Lorenzo; Brugada, Josep; Tercedor, Luis; Tamargo, Juan; Delpón, Eva; Caballero, Ricardo.
Rev. esp. cardiol. (Ed. impr.) ; 72(4): 324-332, abr. 2019. ilus, tab, graf
Artículo en Español | IBECS (España) | ID: ibc-187898

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