Zhizhong Li

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Arthur J Moss, A. Moss, J. Towbin, 1995, Cell.

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

B. Trask, H. Massa, E. Green, 1998, Human Genetics.

Influence of interleukin-28B polymorphism on progression to hepatitis virus-induced hepatocellular carcinoma

G. Yu, Houjie Liang, Zhizhong Li, 2014, Tumor Biology.

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel.

Z. Li, M. Keating, Q. Wang, 1996, Genomics.

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

S. Priori, P. Schwartz, G. Vincent, 1995, Human molecular genetics.