Publications by the researcher in collaboration with Maria Sabater Molina (4)

2016

  1. An R1632C variant in the SCN5A gene causing Brugada syndrome

    Molecular Medicine Reports, Vol. 13, Núm. 6, pp. 4677-4680

2013

  1. A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome

    Clinical Genetics, Vol. 83, Núm. 6, pp. 530-538

  2. Síndrome de Barth en la edad adulta: un caso clínico

    Revista Espanola de Cardiologia

2010

  1. Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3

    Heart, Vol. 96, Núm. 24, pp. 1980-1984