J. Cheng

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

S. Z. Yang, D. Yan, G. Feng, 2008, Clinical genetics.

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

MicroRNA-133b is a key promoter of cervical carcinoma development through the activation of the ERK and AKT1 pathways

P. Dong, Y. Sun, K. Mitchelson, 2012, Oncogene.

Restricted neuronal expression of ubiquitous mitochondrial creatine kinase: Changing patterns in development and with increased activity

T. Woolsey, Z. Khuchua, A. Strauss, 2003, Molecular and Cellular Biochemistry.