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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Published in | Frontiers in genetics Vol. 16; p. 1541333 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
2025
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Subjects | |
Online Access | Get full text |
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