S. Zhai

A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China

L. Lan, J. Guan, Bai-cheng Xu, 2007, Clinical genetics.

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.

AUNX1, a novel locus responsible for X linked recessive auditory and peripheral neuropathy, maps to Xq23–27.3

Q. Z. Li, S. Leal, J. Guan, 2005, Journal of Medical Genetics.

Protective effects of brain-derived neurotrophic factor on the noise-damaged cochlear spiral ganglion

N. Yu, M. Fan, Q. Chen, 2010, The Journal of Laryngology & Otology.

Review of experimental and clinical studies of autoimmune sensorineural hearing loss.

S. Zhai, 2015, Minerva medica.