Rongguang Wang

Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss.

P. Dai, Huijun Yuan, Jianzhong Li, 2011, Journal of genetics and genomics = Yi chuan xue bao.

Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China

J. Chen, X. Liu, D. Yan, 2011, Journal of Human Genetics.

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).

V. Sheffield, J. Bishop, D. Scott, 2000, Human molecular genetics.