Q. Sun

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

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

Acute hepatitis C infection with unclear route of transmission.

J. Cheng, L. Zhang, J. Li, 2012, The West Indian medical journal.

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.

Genetic association of hypertension and several other metabolic disorders with Bell’s palsy

Hua-wei Liu, W. Bi, Q. Sun, 2023, Frontiers in genetics.

Diagnosis, differential diagnosis, and treatment for sudden sensorineural hearing loss: Current otolaryngology practices in China

Lisheng Yu, M. Duan, X. Ning, 2023, Frontiers in Neurology.