Login / Signup

Molecular screening of patients with profound hearing loss from Chengdu, China.

Qingqing DaiWei DaiDan WangXia LiuLing ZouJiani ChenHong ZhengJicheng Zhong
Published in: Acta oto-laryngologica (2021)
gene in our study, which is different from other parts of China. And the deaf-related gene mutation spectrums have a distinct age difference.
Keyphrases
  • hearing loss
  • genome wide
  • copy number
  • gene expression
  • autism spectrum disorder