Universidade da Coruña-ko ikertzaileekin lankidetzan egindako argitalpenak (2)

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

  2. p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

    Heart Rhythm, Vol. 10, Núm. 2, pp. 264-272