CRISPR/Cas9-mediated exon skipping to restore premature translation termination in a DFNB4 mouse model
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41434-024-00483-9.pdf
Reference30 articles.
1. Korver AM, Smith RJ, Van Camp G, Schleiss MR, Bitner-Glindzicz MA, Lustig LR, et al. Congenital hearing loss. Nat Rev Dis Prim. 2017;3:16094.
2. Carpena NT, Lee MY. Genetic hearing loss and gene therapy. Genom Inf. 2018;16:e20.
3. Nicolson T. Navigating hereditary hearing loss: pathology of the inner ear. Front Cell Neurosci. 2021;15:660812.
4. Roesch S, Rasp G, Sarikas A, Dossena S. Genetic determinants of non-syndromic enlarged vestibular aqueduct: a review. Audio Res. 2021;11:423–42.
5. Amlal H, Petrovic S, Xu J, Wang Z, Sun X, Barone S, et al. Deletion of the anion exchanger Slc26a4 (pendrin) decreases apical Cl(-)/HCO3(-) exchanger activity and impairs bicarbonate secretion in kidney collecting duct. Am J Physiol Cell Physiol. 2010;299:C33–41.
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