A novel SCN5A gene mutation (del D1790) associated with congenital long QT syndrome.;

The aim of the present study was to investigate single nucleotide polymorphism (SNP) in SCN5A gene and the distribution of these identi.

Objective To investigate if there is SCN5A gene mutation in sudden unexplained nocturnal death syndrome(SUNDS) cases in Chinese Han nationality population.

Detection of a novel SCN5A gene mutation(G1712C) in patients with asymptomatic Burgada syndrome;

Functional Analysis of Transcriptional Regulation of Intron 1 +204 bp-+785 bp in Rat SCN5A Gene;

Methods Polymerase chain reaction and DNA sequencing were used to screen for KCNQ1, KCNH2, KCNE1, and SCN5A mutation.

Nav1.5 Na~+ Channels in Human Brain Are Encoded by New Variants of Nav1.5/SCN5A;

Study of the Preparation and the Characteristics of pRc/CMV-BChE Gene-chitosan nanoparticles ①;

Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene;

Study on gene chip of leiomyoma of uterus;