Publicacións nas que colabora con 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