Pathophysiology of genetic hearing loss caused by prestin variant: Considerations for future gene therapy
Author:
Affiliation:
1. Department of Physiology The University of Auckland Auckland New Zealand
2. Eisdell Moore Centre The University of Auckland Auckland New Zealand
Funder
Auckland Medical Research Foundation
Publisher
Wiley
Link
https://physoc.onlinelibrary.wiley.com/doi/pdf/10.1113/JP286697
Reference5 articles.
1. Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2
2. AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial
3. The auditory phenotype of children harboring mutations in the prestin gene
4. The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss
5. Prestin’s fast motor kinetics is essential for mammalian cochlear amplification
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