Outcomes of cochlear implants in patients with PCDH15 mutations: a clinical study

To explore molecular diagnoses in cochlear implantation (CI) recipients and evaluate CI outcomes in patients with mutations. Whole-exome sequencing and biomedical informatics were used to identify potential genetic causes in 467 individuals with congenital sensorineural hearing loss. We reviewed six...

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Bibliographic Details
Published inFrontiers in genetics Vol. 16; p. 1541333
Main Authors Bi, Qingling, Chen, Zhongyan, Kang, Baoling, Lv, Yong, Yuan, Yongyi, Liu, Yang, Liu, Jianfeng, Li, Yuan
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 2025
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