Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel.
对 248 例 Brugada 病患者进行分子遗传学和功能异常分析,发现 TRPM4 通道存在 11 个突变
期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0054131
Liu Hui, Chatel Stéphanie, Simard Christophe, Syam Ninda, Salle Laurent, Probst Vincent, Morel Julie, Millat Gilles, Lopez Michel, Abriel Hugues, Schott Jean-Jacques, Guinamard Romain, Bouvagnet Patrice