Viral vectors for gene delivery to the inner ear

Volume: 394, Pages: 107927 - 107927
Published: Sep 1, 2020
Abstract
Gene therapy using virus vectors to treat hereditary diseases has made remarkable progress in the past decade. There are FDA-approved products for ex-vivo gene therapy for diseases such as immunodeficiencies (e.g., SCID), and in vivo gene therapy for a rare blindness and neuro-muscular disease. Gene therapy for hereditary hearing loss has picked up pace in the past five years due to progress in understanding disease gene function as well as the...
Paper Details
Title
Viral vectors for gene delivery to the inner ear
Published Date
Sep 1, 2020
Volume
394
Pages
107927 - 107927
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