Publicacions en col·laboració amb investigadors/es de Hospital Universitario Virgen de las Nieves (4)

2023

  1. A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 120

2019

  1. Digenic Heterozigosity in SCN5A and CACNA1C Explains the Variable Expressivity of the Long QT Phenotype in a Spanish Family

    Revista Espanola de Cardiologia, Vol. 72, Núm. 4, pp. 324-332

2013

  1. Functional characterization of a novel frameshift mutation in the c-terminus of the nav1.5 channel underlying a brugada syndrome with variable expression in a spanish family

    PLoS ONE, Vol. 8, Núm. 11

2011

  1. Functional effects of a missense mutation in HERG associated with type 2 long QT syndrome

    Heart Rhythm, Vol. 8, Núm. 3, pp. 463-470