Hair cell-specific Myo15 promoter-mediated gene therapy rescues hearing in DFNB9 mouse model
Adeno-associated viral (AAV) vectors are increasingly used as vehicles for gene delivery to treat hearing loss. However, lack of specificity of the transgene expression may lead to overexpression of the transgene in nontarget tissues. In this study, we evaluated the expression efficiency and specifi...
| Published in: | Molecular Therapy: Nucleic Acids |
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| Main Authors: | , , , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-03-01
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| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2162253124000222 |
